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nsv6771142

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,381

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 32 studies. See in: genome view    
    Submitted genomic23,519,505-23,521,885Question Mark
    Overlapping variant regions from other studies: 158 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):23,519,614-23,521,994Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6771142Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr523,519,50523,521,885
    nsv6771142RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr523,519,61423,521,994

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18700067duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18700067Submitted genomicNC_000005.10:g.235
    19505_23521885dup
    GRCh38 (hg38)NC_000005.10Chr523,519,50523,521,885
    nssv18700067RemappedPerfectNC_000005.9:g.2351
    9614_23521994dup
    GRCh37.p13First PassNC_000005.9Chr523,519,61423,521,994

    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)
    nssv187000671.8e-054265314
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