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nsv6621189

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:102,950

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 475 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):55,891,613-55,994,562Question Mark
Overlapping variant regions from other studies: 478 SVs from 66 studies. See in: genome view    
Submitted genomic55,659,089-55,762,038Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6621189RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1155,891,61355,994,562
nsv6621189Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1155,659,08955,762,038

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18289431deletionOSC3451SNP arrayProbe signal intensity6

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18289431RemappedPerfectNC_000011.10:g.(?_
55891613)_(5599456
2_?)del
GRCh38.p12First PassNC_000011.10Chr1155,891,61355,994,562
nssv18289431Submitted genomicNC_000011.9:g.(?_5
5659089)_(55762038
_?)del
GRCh37 (hg19)NC_000011.9Chr1155,659,08955,762,038

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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