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nsv5509957

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,051

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 236 SVs from 25 studies. See in: genome view    
Submitted genomic110,538,793-110,539,843Question Mark
Overlapping variant regions from other studies: 236 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):111,191,140-111,192,190Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509957Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13110,538,793110,539,843
nsv5509957RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13111,191,140111,192,190

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17694170deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17694170Submitted genomicNC_000013.11:g.110
538793_110539843de
l
GRCh38 (hg38)NC_000013.11Chr13110,538,793110,539,843
nssv17694170RemappedPerfectNC_000013.10:g.111
191140_111192190de
l
GRCh37.p13First PassNC_000013.10Chr13111,191,140111,192,190

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)
nssv17694170<0.00116404
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