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nsv6204502

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 20 studies. See in: genome view    
Submitted genomic125,493,462-125,493,511Question Mark
Overlapping variant regions from other studies: 160 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):125,363,358-125,363,407Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6204502Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11125,493,462125,493,511
nsv6204502RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11125,363,358125,363,407

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17902454deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17902454Submitted genomicNC_000011.10:g.125
493462_125493511de
l
GRCh38 (hg38)NC_000011.10Chr11125,493,462125,493,511
nssv17902454RemappedPerfectNC_000011.9:g.1253
63358_125363407del
GRCh37.p13First PassNC_000011.9Chr11125,363,358125,363,407

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)
nssv17902454<0.00112254
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