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nsv4330538

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,332,466

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 14105 SVs from 26 studies. See in: genome view    
Remapped(Score: Good):93,757,526-113,089,991Question Mark
Overlapping variant regions from other studies: 14025 SVs from 26 studies. See in: genome view    
Submitted genomic94,223,082-113,632,613Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4330538RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr193,757,526113,089,991
nsv4330538Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr194,223,082113,632,613

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090146inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090146RemappedGoodNC_000001.11:g.937
57526_113089991inv
GRCh38.p12First PassNC_000001.11Chr193,757,526113,089,991
nssv16090146Submitted genomicNC_000001.10:g.942
23082_113632613inv
GRCh37.p13NC_000001.10Chr194,223,082113,632,613

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)
nssv160901464.6e-005121694
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