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esv2421332

  • Variant Calls:47
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34,552

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 654 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):131,313,063-131,347,614Question Mark
Overlapping variant regions from other studies: 654 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):131,797,608-131,832,159Question Mark
Overlapping variant regions from other studies: 249 SVs from 26 studies. See in: genome view    
Submitted genomic130,363,561-130,398,112Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2421332RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12131,313,063131,347,614
esv2421332RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12131,797,608131,832,159
esv2421332Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr12130,363,561130,398,112

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
essv5004711deletionNA19446SNP arraySNP genotyping analysis1147
essv5005768deletionNA21686SNP arraySNP genotyping analysis1149
essv5012016deletionNA18563SNP arraySNP genotyping analysis1127
essv5020535deletionNA19316SNP arraySNP genotyping analysis1130
essv5021716deletionNA07022SNP arraySNP genotyping analysis1142
essv5022471deletionNA21384SNP arraySNP genotyping analysis1131
essv5024238deletionNA19221SNP arraySNP genotyping analysis1148
essv5024540deletionNA19760SNP arraySNP genotyping analysis1143
essv5026781deletionNA21632SNP arraySNP genotyping analysis1142
essv5027186deletionNA19473SNP arraySNP genotyping analysis1152
essv5032531deletionNA18975SNP arraySNP genotyping analysis1141
essv5039419deletionNA19332SNP arraySNP genotyping analysis1141
essv5042481deletionNA20300SNP arraySNP genotyping analysis1137
essv5043385deletionNA21307SNP arraySNP genotyping analysis1140
essv5054729deletionNA18981SNP arraySNP genotyping analysis1124
essv5055810deletionNA18160SNP arraySNP genotyping analysis1137
essv5069145deletionNA21650SNP arraySNP genotyping analysis1145
essv5071957deletionNA19778SNP arraySNP genotyping analysis1125
essv5072458deletionNA18945SNP arraySNP genotyping analysis1137
essv5075476deletionNA19154SNP arraySNP genotyping analysis1128
essv5076807deletionNA21478SNP arraySNP genotyping analysis1132
essv5079246deletionNA18557SNP arraySNP genotyping analysis1122
essv5087135deletionNA19223SNP arraySNP genotyping analysis1144
essv5089975deletionNA19390SNP arraySNP genotyping analysis1147
essv5094822deletionNA19439SNP arraySNP genotyping analysis1151
essv5102500deletionNA18577SNP arraySNP genotyping analysis1125
essv5104415deletionNA19153SNP arraySNP genotyping analysis1114
essv5109349deletionNA19763SNP arraySNP genotyping analysis1125
essv5111954deletionNA21480SNP arraySNP genotyping analysis1138
essv5112417deletionNA19901SNP arraySNP genotyping analysis1145
essv5115841deletionNA21580SNP arraySNP genotyping analysis1136
essv5116780deletionNA19750SNP arraySNP genotyping analysis1124
essv5121920deletionNA18632SNP arraySNP genotyping analysis1131
essv5123134deletionNA21389SNP arraySNP genotyping analysis1138
essv5127951deletionNA19751SNP arraySNP genotyping analysis1144
essv5136320deletionNA19214SNP arraySNP genotyping analysis1137
essv5138497deletionNA20785SNP arraySNP genotyping analysis1133
essv5142792deletionNA21387SNP arraySNP genotyping analysis1115
essv5143873deletionNA19761SNP arraySNP genotyping analysis1131
essv5145107deletionNA19371SNP arraySNP genotyping analysis1142
essv5149292deletionNA20754SNP arraySNP genotyping analysis1123
essv5150775deletionNA19777SNP arraySNP genotyping analysis1129
essv5151276deletionNA20509SNP arraySNP genotyping analysis1145
essv5154097deletionNA21385SNP arraySNP genotyping analysis1135
essv5154879deletionNA19448SNP arraySNP genotyping analysis1142
essv5156714deletionNA19375SNP arraySNP genotyping analysis1155
essv5159496deletionNA18682SNP arraySNP genotyping analysis1138

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5004711RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5005768RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5012016RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5020535RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5021716RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5022471RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5024238RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5024540RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5026781RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5027186RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5032531RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5039419RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5042481RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5043385RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5054729RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5055810RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5069145RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5071957RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5072458RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5075476RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5076807RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5079246RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5087135RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5089975RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5094822RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5102500RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5104415RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5109349RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5111954RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5112417RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5115841RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5116780RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5121920RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5123134RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5127951RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5136320RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5138497RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5142792RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5143873RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5145107RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5149292RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5150775RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5151276RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5154097RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5154879RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5156714RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5159496RemappedPerfectNC_000012.12:g.(?_
131313063)_(131347
614_?)del
GRCh38.p12First PassNC_000012.12Chr12131,313,063131,347,614
essv5004711RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5005768RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5012016RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5020535RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5021716RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5022471RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5024238RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5024540RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5026781RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5027186RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5032531RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5039419RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5042481RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5043385RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5054729RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5055810RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5069145RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5071957RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5072458RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5075476RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5076807RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5079246RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5087135RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5089975RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5094822RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5102500RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5104415RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5109349RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5111954RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5112417RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5115841RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5116780RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5121920RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5123134RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5127951RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5136320RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5138497RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5142792RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5143873RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5145107RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5149292RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5150775RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5151276RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5154097RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5154879RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5156714RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5159496RemappedPerfectNC_000012.11:g.(?_
131797608)_(131832
159_?)del
GRCh37.p13First PassNC_000012.11Chr12131,797,608131,832,159
essv5004711Submitted genomicNC_000012.10:g.(?_
130363561)_(130398
112_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,398,112
essv5005768Submitted genomicNC_000012.10:g.(?_
130363561)_(130398
112_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,398,112
essv5012016Submitted genomicNC_000012.10:g.(?_
130363561)_(130398
112_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,398,112
essv5020535Submitted genomicNC_000012.10:g.(?_
130363561)_(130398
112_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,398,112
essv5021716Submitted genomicNC_000012.10:g.(?_
130363561)_(130398
112_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,398,112
essv5022471Submitted genomicNC_000012.10:g.(?_
130363561)_(130398
112_?)del
NCBI36 (hg18)NC_000012.10Chr12130,363,561130,398,112
Showing 100 of 141

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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