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nsv6995210

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:591,943

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2155 SVs from 77 studies. See in: genome view    
    Submitted genomic38,770,587-39,362,529Question Mark
    Overlapping variant regions from other studies: 2154 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):36,926,840-37,518,782Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995210Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1738,770,58739,362,529
    nsv6995210RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1736,926,84037,518,782

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628680duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628680Submitted genomicNC_000017.11:g.387
    70587_39362529dup
    GRCh38 (hg38)NC_000017.11Chr1738,770,58739,362,529
    nssv18628680RemappedPerfectNC_000017.10:g.369
    26840_37518782dup
    GRCh37.p13First PassNC_000017.10Chr1736,926,84037,518,782

    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)
    nssv186286807e-062273550
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