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nsv6468374

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:163

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 27 studies. See in: genome view    
    Submitted genomic74,237,006-74,237,168Question Mark
    Overlapping variant regions from other studies: 95 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):73,948,051-73,948,213Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6468374Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,237,00674,237,168
    nsv6468374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,948,05173,948,213

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17993588deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17993588Submitted genomicNC_000011.10:g.742
    37006_74237168del
    GRCh38 (hg38)NC_000011.10Chr1174,237,00674,237,168
    nssv17993588RemappedPerfectNC_000011.9:g.7394
    8051_73948213del
    GRCh37.p13First PassNC_000011.9Chr1173,948,05173,948,213

    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)
    nssv179935880.00933639238
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