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nsv5510079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:577

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 187 SVs from 17 studies. See in: genome view    
Submitted genomic129,862,841-129,863,417Question Mark
Overlapping variant regions from other studies: 187 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):129,732,736-129,733,312Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5510079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11129,862,841129,863,417
nsv5510079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11129,732,736129,733,312

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052682deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052682Submitted genomicNC_000011.10:g.129
862841_129863417de
l
GRCh38 (hg38)NC_000011.10Chr11129,862,841129,863,417
nssv17052682RemappedPerfectNC_000011.9:g.1297
32736_129733312del
GRCh37.p13First PassNC_000011.9Chr11129,732,736129,733,312

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)
nssv17052682<0.00136404
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