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nsv5451132

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:335

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 131 SVs from 34 studies. See in: genome view    
Submitted genomic125,297,419-125,297,753Question Mark
Overlapping variant regions from other studies: 131 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):125,016,263-125,016,597Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5451132Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3125,297,419125,297,753
nsv5451132RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3125,016,263125,016,597

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16938777deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16938777Submitted genomicNC_000003.12:g.125
297419_125297753de
l
GRCh38 (hg38)NC_000003.12Chr3125,297,419125,297,753
nssv16938777RemappedPerfectNC_000003.11:g.125
016263_125016597de
l
GRCh37.p13First PassNC_000003.11Chr3125,016,263125,016,597

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)
nssv169387770.0291886404
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