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nsv6977817

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:261,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 992 SVs from 72 studies. See in: genome view    
    Submitted genomic103,673,601-103,934,800Question Mark
    Overlapping variant regions from other studies: 992 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):104,139,938-104,401,137Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977817Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14103,673,601103,934,800
    nsv6977817RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14104,139,938104,401,137

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18612962duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18612962Submitted genomicNC_000014.9:g.1036
    73601_103934800dup
    GRCh38 (hg38)NC_000014.9Chr14103,673,601103,934,800
    nssv18612962RemappedPerfectNC_000014.8:g.1041
    39938_104401137dup
    GRCh37.p13First PassNC_000014.8Chr14104,139,938104,401,137

    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)
    nssv18612962<0.00128264184
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