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nsv5548151

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
Submitted genomic179,129,579-179,129,629Question Mark
Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):178,847,367-178,847,417Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548151Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3179,129,579179,129,629
nsv5548151RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3178,847,367178,847,417

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942998insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942998Submitted genomicNC_000003.12:g.179
129579_179129629in
s50
GRCh38 (hg38)NC_000003.12Chr3179,129,579179,129,629
nssv16942998RemappedPerfectNC_000003.11:g.178
847367_178847417in
s50
GRCh37.p13First PassNC_000003.11Chr3178,847,367178,847,417

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)
nssv16942998<0.00116404
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