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nsv5454405

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,362

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 44 studies. See in: genome view    
Submitted genomic118,322,561-118,325,922Question Mark
Overlapping variant regions from other studies: 154 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):119,243,716-119,247,077Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5454405Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4118,322,561118,325,922
nsv5454405RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4119,243,716119,247,077

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16954062deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16954062Submitted genomicNC_000004.12:g.118
322561_118325922de
l
GRCh38 (hg38)NC_000004.12Chr4118,322,561118,325,922
nssv16954062RemappedPerfectNC_000004.11:g.119
243716_119247077de
l
GRCh37.p13First PassNC_000004.11Chr4119,243,716119,247,077

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)
nssv169540620.003186404
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