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nsv4313384

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,499,276

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 17610 SVs from 25 studies. See in: genome view    
Remapped(Score: Pass):36,819,153-58,318,428Question Mark
Overlapping variant regions from other studies: 15313 SVs from 25 studies. See in: genome view    
Submitted genomic37,108,081-60,078,188Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4313384RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1036,819,15358,318,428
nsv4313384Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1037,108,08160,078,188

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091028inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091028RemappedPassNC_000010.11:g.368
19153_58318428inv
GRCh38.p12First PassNC_000010.11Chr1036,819,15358,318,428
nssv16091028Submitted genomicNC_000010.10:g.371
08081_60078188inv
GRCh37.p13NC_000010.10Chr1037,108,08160,078,188

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)
nssv16091028<0.001321694
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