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nsv6193835

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 159 SVs from 20 studies. See in: genome view    
Submitted genomic125,493,457-125,493,508Question Mark
Overlapping variant regions from other studies: 159 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):125,363,353-125,363,404Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6193835Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11125,493,457125,493,508
nsv6193835RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11125,363,353125,363,404

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17916060deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17916060Submitted genomicNC_000011.10:g.125
493457_125493508de
l
GRCh38 (hg38)NC_000011.10Chr11125,493,457125,493,508
nssv17916060RemappedPerfectNC_000011.9:g.1253
63353_125363404del
GRCh37.p13First PassNC_000011.9Chr11125,363,353125,363,404

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)
nssv17916060<0.00112254
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