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nsv6763717

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:772,996

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2103 SVs from 88 studies. See in: genome view    
    Submitted genomic96,412,203-97,185,198Question Mark
    Overlapping variant regions from other studies: 2104 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):95,747,907-96,520,902Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6763717Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr596,412,20397,185,198
    nsv6763717RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr595,747,90796,520,902

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708215duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708215Submitted genomicNC_000005.10:g.964
    12203_97185198dup
    GRCh38 (hg38)NC_000005.10Chr596,412,20397,185,198
    nssv18708215RemappedPerfectNC_000005.9:g.9574
    7907_96520902dup
    GRCh37.p13First PassNC_000005.9Chr595,747,90796,520,902

    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)
    nssv187082154e-061275712
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