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nsv5503923

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:801

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 168 SVs from 25 studies. See in: genome view    
Submitted genomic100,615,568-100,616,368Question Mark
Overlapping variant regions from other studies: 168 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):101,267,822-101,268,622Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503923Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13100,615,568100,616,368
nsv5503923RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13101,267,822101,268,622

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17691220deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17691220Submitted genomicNC_000013.11:g.100
615568_100616368de
l
GRCh38 (hg38)NC_000013.11Chr13100,615,568100,616,368
nssv17691220RemappedPerfectNC_000013.10:g.101
267822_101268622de
l
GRCh37.p13First PassNC_000013.10Chr13101,267,822101,268,622

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)
nssv17691220<0.00116404
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