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nsv1161343

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176,340

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 570 SVs from 62 studies. See in: genome view    
Remapped(Score: Good):21,861,465-22,037,804Question Mark
Overlapping variant regions from other studies: 570 SVs from 62 studies. See in: genome view    
Submitted genomic21,861,696-22,038,033Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv1161343RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr621,861,46521,861,46522,037,80422,037,804
nsv1161343Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr621,861,69621,863,89922,036,86722,038,033

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv4034225deletionSNP arrayProbe signal intensity1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv4034225RemappedGoodNC_000006.12:g.(21
861465_21861465)_(
22037804_22037804)
del
GRCh38.p12First PassNC_000006.12Chr621,861,46521,861,46522,037,80422,037,804
nssv4034225Submitted genomicNC_000006.11:g.(21
861696_21863899)_(
22036867_22038033)
del
GRCh37 (hg19)NC_000006.11Chr621,861,69621,863,89922,036,86722,038,033

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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