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nsv6130535

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):40,024,244-40,024,279Question Mark
Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
Submitted genomic40,316,445-40,316,480Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6130535RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1540,024,24440,024,279
nsv6130535Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000015.9Chr1540,316,44540,316,480

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17964110insertionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17964110RemappedPerfectNC_000015.10:g.400
24244_40024279ins?
GRCh38.p12First PassNC_000015.10Chr1540,024,24440,024,279
nssv17964110Submitted genomicNC_000015.9:g.4031
6445_40316480ins?
GRCh37 (hg19)NC_000015.9Chr1540,316,44540,316,480

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv179641100.0161046404
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