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nsv4325802

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,095,194

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 27079 SVs from 24 studies. See in: genome view    
Remapped(Score: Good):69,787,030-109,882,223Question Mark
Overlapping variant regions from other studies: 27061 SVs from 24 studies. See in: genome view    
Submitted genomic70,180,810-110,320,028Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4325802RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1269,787,030109,882,223
nsv4325802Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1270,180,810110,320,028

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090794inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090794RemappedGoodNC_000012.12:g.697
87030_109882223inv
GRCh38.p12First PassNC_000012.12Chr1269,787,030109,882,223
nssv16090794Submitted genomicNC_000012.11:g.701
80810_110320028inv
GRCh37.p13NC_000012.11Chr1270,180,810110,320,028

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)
nssv160907944.6e-005121694
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