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nsv6531783

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 19 studies. See in: genome view    
    Submitted genomic43,534,901-43,535,300Question Mark
    Overlapping variant regions from other studies: 110 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):44,039,053-44,039,452Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6531783Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1943,534,90143,535,300
    nsv6531783RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1944,039,05344,039,452

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18048111deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18048111Submitted genomicNC_000019.10:g.435
    34901_43535300del
    GRCh38 (hg38)NC_000019.10Chr1943,534,90143,535,300
    nssv18048111RemappedPerfectNC_000019.9:g.4403
    9053_44039452del
    GRCh37.p13First PassNC_000019.9Chr1944,039,05344,039,452

    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)
    nssv180481110.072279538758
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