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nsv6894655

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,190

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 22 studies. See in: genome view    
    Submitted genomic17,814,824-17,816,013Question Mark
    Overlapping variant regions from other studies: 4 SVs from 4 studies. See in: genome view    
    Remapped(Score: Perfect):243,615-244,804Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6894655Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1017,814,82417,816,013
    nsv6894655RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315932.1Chr10|NW_0
    03315932.1
    243,615244,804

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586051duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586051Submitted genomicNC_000010.11:g.178
    14824_17816013dup
    GRCh38 (hg38)NC_000010.11Chr1017,814,82417,816,013
    nssv18586051RemappedPerfectNW_003315932.1:g.2
    43615_244804dup
    GRCh37.p13First PassNW_003315932.1Chr10|NW_0
    03315932.1
    243,615244,804

    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)
    nssv185860517e-0516251010
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