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nsv6674310

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,344

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 21 studies. See in: genome view    
    Submitted genomic64,930,540-64,933,883Question Mark
    Overlapping variant regions from other studies: 105 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):65,157,674-65,161,017Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6674310Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr264,930,54064,933,883
    nsv6674310RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr265,157,67465,161,017

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18468247deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18468247Submitted genomicNC_000002.12:g.649
    30540_64933883del
    GRCh38 (hg38)NC_000002.12Chr264,930,54064,933,883
    nssv18468247RemappedPerfectNC_000002.11:g.651
    57674_65161017del
    GRCh37.p13First PassNC_000002.11Chr265,157,67465,161,017

    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)
    nssv184682474e-061276118
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