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nsv4327204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,188,715

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 17616 SVs from 25 studies. See in: genome view    
Remapped(Score: Good):156,253,235-186,441,949Question Mark
Overlapping variant regions from other studies: 17609 SVs from 25 studies. See in: genome view    
Submitted genomic156,223,026-186,411,081Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4327204RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1156,253,235186,441,949
nsv4327204Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1156,223,026186,411,081

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090158inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090158RemappedGoodNC_000001.11:g.156
253235_186441949in
v
GRCh38.p12First PassNC_000001.11Chr1156,253,235186,441,949
nssv16090158Submitted genomicNC_000001.10:g.156
223026_186411081in
v
GRCh37.p13NC_000001.10Chr1156,223,026186,411,081

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)
nssv160901584.6e-005121694
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