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nsv6803596

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 296 SVs from 54 studies. See in: genome view    
    Submitted genomic1,613,301-1,636,400Question Mark
    Overlapping variant regions from other studies: 296 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):1,652,937-1,676,036Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6803596Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr71,613,3011,636,400
    nsv6803596RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr71,652,9371,676,036

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18537834deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18537834Submitted genomicNC_000007.14:g.161
    3301_1636400del
    GRCh38 (hg38)NC_000007.14Chr71,613,3011,636,400
    nssv18537834RemappedPerfectNC_000007.13:g.165
    2937_1676036del
    GRCh37.p13First PassNC_000007.13Chr71,652,9371,676,036

    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)
    nssv18537834<0.00142253454
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