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nsv6836699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:416

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 27 studies. See in: genome view    
    Submitted genomic105,268,040-105,268,455Question Mark
    Overlapping variant regions from other studies: 139 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):104,908,487-104,908,902Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6836699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7105,268,040105,268,455
    nsv6836699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7104,908,487104,908,902

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18717656duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18717656Submitted genomicNC_000007.14:g.105
    268040_105268455du
    p
    GRCh38 (hg38)NC_000007.14Chr7105,268,040105,268,455
    nssv18717656RemappedPerfectNC_000007.13:g.104
    908487_104908902du
    p
    GRCh37.p13First PassNC_000007.13Chr7104,908,487104,908,902

    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)
    nssv187176564e-061238310
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