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nsv4326932

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58,285,085

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 37882 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):34,707,889-92,992,973Question Mark
Overlapping variant regions from other studies: 37879 SVs from 26 studies. See in: genome view    
Submitted genomic35,173,490-93,458,530Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4326932RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr134,707,88992,992,973
nsv4326932Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr135,173,49093,458,530

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090122inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090122RemappedPerfectNC_000001.11:g.347
07889_92992973inv
GRCh38.p12First PassNC_000001.11Chr134,707,88992,992,973
nssv16090122Submitted genomicNC_000001.10:g.351
73490_93458530inv
GRCh37.p13NC_000001.10Chr135,173,49093,458,530

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)
nssv160901224.6e-005121694
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