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nsv6732064

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:188,031

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 904 SVs from 70 studies. See in: genome view    
    Submitted genomic4,174,095-4,362,125Question Mark
    Overlapping variant regions from other studies: 904 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):4,175,822-4,363,852Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6732064Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr44,174,0954,362,125
    nsv6732064RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr44,175,8224,363,852

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18498372deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18498372Submitted genomicNC_000004.12:g.417
    4095_4362125del
    GRCh38 (hg38)NC_000004.12Chr44,174,0954,362,125
    nssv18498372RemappedPerfectNC_000004.11:g.417
    5822_4363852del
    GRCh37.p13First PassNC_000004.11Chr44,175,8224,363,852

    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)
    nssv184983724e-061276070
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