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nsv7051268

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,352,328

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5043 SVs from 107 studies. See in: genome view    
    Submitted genomic37,000,362-39,352,689Question Mark
    Overlapping variant regions from other studies: 5043 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):37,041,853-39,394,180Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051268Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr337,000,36239,352,689
    nsv7051268RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr337,041,85339,394,180

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771671inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771671Submitted genomicNC_000003.12:g.370
    00362_39352689inv
    GRCh38 (hg38)NC_000003.12Chr337,000,36239,352,689
    nssv18771671RemappedPerfectNC_000003.11:g.370
    41853_39394180inv
    GRCh37.p13First PassNC_000003.11Chr337,041,85339,394,180

    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)
    nssv18771671<0.00135272382
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