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nsv6826512

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,580,468

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4339 SVs from 106 studies. See in: genome view    
    Submitted genomic89,228,365-90,808,832Question Mark
    Overlapping variant regions from other studies: 4340 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):88,857,679-90,438,147Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6826512Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr789,228,36590,808,832
    nsv6826512RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr788,857,67990,438,147

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18729003duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18729003Submitted genomicNC_000007.14:g.892
    28365_90808832dup
    GRCh38 (hg38)NC_000007.14Chr789,228,36590,808,832
    nssv18729003RemappedPerfectNC_000007.13:g.888
    57679_90438147dup
    GRCh37.p13First PassNC_000007.13Chr788,857,67990,438,147

    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)
    nssv187290034e-061275262
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