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nsv6146143

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,957

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 48 studies. See in: genome view    
Submitted genomic71,688,336-71,699,292Question Mark
Overlapping variant regions from other studies: 162 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):71,980,675-71,991,631Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6146143Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1571,688,33671,699,292
nsv6146143RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1571,980,67571,991,631

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702396deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702396Submitted genomicNC_000015.10:g.716
88336_71699292del
GRCh38 (hg38)NC_000015.10Chr1571,688,33671,699,292
nssv17702396RemappedPerfectNC_000015.9:g.7198
0675_71991631del
GRCh37.p13First PassNC_000015.9Chr1571,980,67571,991,631

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)
nssv17702396<0.00136404
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