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nsv6147491

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,130

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 25 studies. See in: genome view    
Submitted genomic35,697,613-35,708,742Question Mark
Overlapping variant regions from other studies: 96 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):35,719,161-35,730,290Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147491Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1135,697,61335,708,742
nsv6147491RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1135,719,16135,730,290

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17044246mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17044246Submitted genomicNC_000011.10:g.356
97613_35708742del
GRCh38 (hg38)NC_000011.10Chr1135,697,61335,708,742
nssv17044246RemappedPerfectNC_000011.9:g.3571
9161_35730290del
GRCh37.p13First PassNC_000011.9Chr1135,719,16135,730,290

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv170442460.015986404
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