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nsv6961308

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:436,981

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2075 SVs from 89 studies. See in: genome view    
    Submitted genomic104,494,808-104,931,788Question Mark
    Overlapping variant regions from other studies: 2074 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):104,961,145-105,398,125Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961308Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14104,494,808104,931,788
    nsv6961308RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14104,961,145105,398,125

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18613633duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18613633Submitted genomicNC_000014.9:g.1044
    94808_104931788dup
    GRCh38 (hg38)NC_000014.9Chr14104,494,808104,931,788
    nssv18613633RemappedPerfectNC_000014.8:g.1049
    61145_105398125dup
    GRCh37.p13First PassNC_000014.8Chr14104,961,145105,398,125

    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)
    nssv186136334e-061275646
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