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esv2760755

  • Variant Calls:49
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,248

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 456 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):27,487,981-27,504,228Question Mark
Overlapping variant regions from other studies: 456 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):27,640,914-27,657,161Question Mark
Overlapping variant regions from other studies: 184 SVs from 26 studies. See in: genome view    
Submitted genomic27,532,181-27,548,428Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2760755RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1227,487,98127,504,228
esv2760755RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1227,640,91427,657,161
esv2760755Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr1227,532,18127,548,428

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv6997071copy number lossSW_1071SNP arraySNP genotyping analysis35
essv6997072copy number lossSW_0758SNP arraySNP genotyping analysis35
essv6997073copy number lossSW_0004SNP arraySNP genotyping analysis44
essv6997074copy number lossSW_0073SNP arraySNP genotyping analysis31
essv6997075copy number lossSW_0370SNP arraySNP genotyping analysis36
essv6997076copy number lossSW_1000SNP arraySNP genotyping analysis42
essv6997079copy number lossSW_1231SNP arraySNP genotyping analysis21
essv6997080copy number lossSW_1233SNP arraySNP genotyping analysis24
essv6997081copy number lossSW_1327SNP arraySNP genotyping analysis38
essv6997082copy number lossSW_1367SNP arraySNP genotyping analysis31
essv6997083copy number lossSW_1374SNP arraySNP genotyping analysis28
essv6997084copy number lossSW_0639SNP arraySNP genotyping analysis58
essv6997085copy number lossSW_0006SNP arraySNP genotyping analysis37
essv6997086copy number lossSW_0118SNP arraySNP genotyping analysis46
essv6997087copy number lossSW_0143SNP arraySNP genotyping analysis22
essv6997088copy number lossSW_0144SNP arraySNP genotyping analysis51
essv6997090copy number lossSW_0158SNP arraySNP genotyping analysis50
essv6997091copy number lossSW_0159SNP arraySNP genotyping analysis52
essv6997092copy number lossSW_0191SNP arraySNP genotyping analysis36
essv6997093copy number lossSW_0339SNP arraySNP genotyping analysis39
essv6997094copy number lossSW_0369SNP arraySNP genotyping analysis24
essv6997095copy number lossSW_0568SNP arraySNP genotyping analysis30
essv6997096copy number lossSW_0603SNP arraySNP genotyping analysis28
essv6997097copy number lossSW_0606SNP arraySNP genotyping analysis46
essv6997098copy number lossSW_0646SNP arraySNP genotyping analysis38
essv6997099copy number lossSW_0653SNP arraySNP genotyping analysis37
essv6997101copy number lossSW_0760SNP arraySNP genotyping analysis44
essv6997102copy number lossSW_0841SNP arraySNP genotyping analysis37
essv6997103copy number lossSW_0891SNP arraySNP genotyping analysis34
essv6997104copy number lossSW_1026SNP arraySNP genotyping analysis48
essv6997105copy number lossSW_1029SNP arraySNP genotyping analysis42
essv6997106copy number lossSW_1089SNP arraySNP genotyping analysis45
essv6997107copy number lossSW_1106SNP arraySNP genotyping analysis34
essv6997108copy number lossSW_1126SNP arraySNP genotyping analysis46
essv6997109copy number lossSW_1132SNP arraySNP genotyping analysis34
essv6997110copy number lossSW_1147SNP arraySNP genotyping analysis41
essv6997112copy number lossSW_1156SNP arraySNP genotyping analysis48
essv6997113copy number lossSW_1197SNP arraySNP genotyping analysis25
essv6997114copy number lossSW_1208SNP arraySNP genotyping analysis38
essv6997115copy number lossSW_1315SNP arraySNP genotyping analysis20
essv6997116copy number lossSW_1322SNP arraySNP genotyping analysis30
essv6997117copy number lossSW_1358SNP arraySNP genotyping analysis36
essv6997118copy number lossSW_1405SNP arraySNP genotyping analysis39
essv6997119copy number lossSW_1412SNP arraySNP genotyping analysis30
essv6997120copy number lossSW_1416SNP arraySNP genotyping analysis36
essv6997121copy number lossSW_1419SNP arraySNP genotyping analysis32
essv6997123copy number lossSW_1457SNP arraySNP genotyping analysis26
essv6997124copy number lossSW_1469SNP arraySNP genotyping analysis43
essv6997125copy number lossSW_1227SNP arraySNP genotyping analysis17

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv6997071RemappedPerfectNC_000012.12:g.(?_
27487981)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,487,98127,498,429
essv6997072RemappedPerfectNC_000012.12:g.(?_
27490257)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,490,25727,498,429
essv6997073RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997074RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997075RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997076RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997079RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997080RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997081RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997082RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997083RemappedPerfectNC_000012.12:g.(?_
27493053)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,498,429
essv6997084RemappedPerfectNC_000012.12:g.(?_
27493053)_(2750422
8_?)del
GRCh38.p12First PassNC_000012.12Chr1227,493,05327,504,228
essv6997085RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997086RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997087RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997088RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997090RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997091RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997092RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997093RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997094RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997095RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997096RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997097RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997098RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997099RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997101RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997102RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997103RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997104RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997105RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997106RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997107RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997108RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997109RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997110RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997112RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997113RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997114RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997115RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997116RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997117RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997118RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997119RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997120RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997121RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997123RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997124RemappedPerfectNC_000012.12:g.(?_
27494808)_(2749842
9_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,498,429
essv6997125RemappedPerfectNC_000012.12:g.(?_
27494808)_(2750422
8_?)del
GRCh38.p12First PassNC_000012.12Chr1227,494,80827,504,228
essv6997071RemappedPerfectNC_000012.11:g.(?_
27640914)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,640,91427,651,362
essv6997072RemappedPerfectNC_000012.11:g.(?_
27643190)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,643,19027,651,362
essv6997073RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997074RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997075RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997076RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997079RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997080RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997081RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997082RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997083RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,651,362
essv6997084RemappedPerfectNC_000012.11:g.(?_
27645986)_(2765716
1_?)del
GRCh37.p13First PassNC_000012.11Chr1227,645,98627,657,161
essv6997085RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997086RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997087RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997088RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997090RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997091RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997092RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997093RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997094RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997095RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997096RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997097RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997098RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997099RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997101RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997102RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997103RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997104RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997105RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997106RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997107RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997108RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997109RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997110RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997112RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997113RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997114RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997115RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997116RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997117RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997118RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997119RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997120RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997121RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997123RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997124RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765136
2_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,651,362
essv6997125RemappedPerfectNC_000012.11:g.(?_
27647741)_(2765716
1_?)del
GRCh37.p13First PassNC_000012.11Chr1227,647,74127,657,161
essv6997071Submitted genomicNC_000012.10:g.(?_
27532181)_(2754262
9_?)del
NCBI36 (hg18)NC_000012.10Chr1227,532,18127,542,629
essv6997072Submitted genomicNC_000012.10:g.(?_
27534457)_(2754262
9_?)del
NCBI36 (hg18)NC_000012.10Chr1227,534,45727,542,629
Showing 100 of 147

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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