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nsv6915763

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,672

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 221 SVs from 52 studies. See in: genome view    
    Submitted genomic4,804,075-4,843,746Question Mark
    Overlapping variant regions from other studies: 221 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):4,825,305-4,864,976Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6915763Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,804,0754,843,746
    nsv6915763RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,825,3054,864,976

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18350238deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18350238Submitted genomicNC_000011.10:g.480
    4075_4843746del
    GRCh38 (hg38)NC_000011.10Chr114,804,0754,843,746
    nssv18350238RemappedPerfectNC_000011.9:g.4825
    305_4864976del
    GRCh37.p13First PassNC_000011.9Chr114,825,3054,864,976

    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)
    nssv183502381.8e-054274926
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