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nsv6769699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:799,372

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2780 SVs from 97 studies. See in: genome view    
    Submitted genomic29,072,356-29,871,727Question Mark
    Overlapping variant regions from other studies: 2782 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):29,072,463-29,871,834Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6769699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr529,072,35629,871,727
    nsv6769699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr529,072,46329,871,834

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703385duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703385Submitted genomicNC_000005.10:g.290
    72356_29871727dup
    GRCh38 (hg38)NC_000005.10Chr529,072,35629,871,727
    nssv18703385RemappedPerfectNC_000005.9:g.2907
    2463_29871834dup
    GRCh37.p13First PassNC_000005.9Chr529,072,46329,871,834

    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)
    nssv187033857e-062273146
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