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nsv4329233

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,434

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 66 SVs from 11 studies. See in: genome view    
Remapped(Score: Perfect):106,352,429-106,416,862Question Mark
Overlapping variant regions from other studies: 66 SVs from 11 studies. See in: genome view    
Submitted genomic106,223,156-106,287,589Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4329233RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11106,352,429106,416,862
nsv4329233Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr11106,223,156106,287,589

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090762inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090762RemappedPerfectNC_000011.10:g.106
352429_106416862in
v
GRCh38.p12First PassNC_000011.10Chr11106,352,429106,416,862
nssv16090762Submitted genomicNC_000011.9:g.1062
23156_106287589inv
GRCh37.p13NC_000011.9Chr11106,223,156106,287,589

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)
nssv160907624.6e-005121694
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