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nsv6622217

  • Variant Calls:27
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,155

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 569 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):83,537,638-83,583,792Question Mark
Overlapping variant regions from other studies: 569 SVs from 69 studies. See in: genome view    
Submitted genomic84,111,773-84,157,927Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6622217RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1383,537,63883,583,792
nsv6622217Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1384,111,77384,157,927

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18282646deletionOSC2103SNP arrayProbe signal intensity6
nssv18282862deletionOSC2267SNP arrayProbe signal intensitynssv18283492
nssv18283564deletionOSC2312SNP arrayProbe signal intensitynssv18283226, nssv18283845, nssv18283563
nssv18283794deletionOSC2278SNP arrayProbe signal intensitynssv18283795
nssv18285021deletionOSC2474SNP arrayProbe signal intensitynssv18283419, nssv18284090, nssv18285022
nssv18285103deletionOSC2524SNP arrayProbe signal intensity8
nssv18286212deletionOSC2902SNP arrayProbe signal intensity7
nssv18287849deletionOSC3152SNP arrayProbe signal intensity10
nssv18287924deletionOSC3200SNP arrayProbe signal intensity9
nssv18288602deletionOSC3280SNP arrayProbe signal intensitynssv18288268
nssv18289079deletionOSC3373SNP arrayProbe signal intensitynssv18289322, nssv18289323
nssv18289520deletionOSC3523SNP arrayProbe signal intensity11
nssv18291427deletionOSC3757SNP arrayProbe signal intensity8
nssv18291949deletionOSC3939SNP arrayProbe signal intensity7
nssv18292445deletionOSC3816SNP arrayProbe signal intensity5
nssv18294914deletionOSC4254SNP arrayProbe signal intensity7
nssv18295939deletionOSC4583SNP arrayProbe signal intensity7
nssv18296629deletionOSC0496SNP arrayProbe signal intensitynssv18296864
nssv18296988deletionOSC4907SNP arrayProbe signal intensitynssv18296989, nssv18296990
nssv18297472deletionOSC4772SNP arrayProbe signal intensitynssv18297473, nssv18296567, nssv18296566
nssv18298176deletionOSC5104SNP arrayProbe signal intensity8
nssv18298797deletionOSC0518SNP arrayProbe signal intensity7
nssv18310274deletionOSC0754SNP arrayProbe signal intensity8
nssv18322066deletionOSC1192SNP arrayProbe signal intensitynssv18321782, nssv18322067
nssv18322722deletionOSC1384SNP arrayProbe signal intensity6
nssv18324008deletionOSC1653SNP arrayProbe signal intensity7
nssv18324431deletionOSC1747SNP arrayProbe signal intensity8

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18282646RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18282862RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18283564RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18283794RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18285021RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18285103RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18286212RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18287849RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18287924RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18288602RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18289079RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18289520RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18291427RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18291949RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18292445RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18294914RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18295939RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18296629RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18296988RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18297472RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18298176RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18298797RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18310274RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18322066RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18322722RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18324008RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18324431RemappedPerfectNC_000013.11:g.(?_
83537638)_(8358379
2_?)del
GRCh38.p12First PassNC_000013.11Chr1383,537,63883,583,792
nssv18282646Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18282862Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18283564Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18283794Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18285021Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18285103Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18286212Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18287849Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18287924Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18288602Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18289079Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18289520Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18291427Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18291949Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18292445Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18294914Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18295939Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18296629Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18296988Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18297472Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18298176Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18298797Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18310274Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18322066Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18322722Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18324008Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927
nssv18324431Submitted genomicNC_000013.10:g.(?_
84111773)_(8415792
7_?)del
GRCh37 (hg19)NC_000013.10Chr1384,111,77384,157,927

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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