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nsv6910853

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:124,579

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 690 SVs from 74 studies. See in: genome view    
    Submitted genomic4,496,473-4,621,051Question Mark
    Overlapping variant regions from other studies: 690 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):4,517,703-4,642,281Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6910853Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,496,4734,621,051
    nsv6910853RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,517,7034,642,281

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18345834deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18345834Submitted genomicNC_000011.10:g.449
    6473_4621051del
    GRCh38 (hg38)NC_000011.10Chr114,496,4734,621,051
    nssv18345834RemappedPerfectNC_000011.9:g.4517
    703_4642281del
    GRCh37.p13First PassNC_000011.9Chr114,517,7034,642,281

    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)
    nssv183458344e-061276214
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