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nsv6715310

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:172

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 71 SVs from 15 studies. See in: genome view    
    Submitted genomic43,407,412-43,407,583Question Mark
    Overlapping variant regions from other studies: 71 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):43,448,904-43,449,075Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6715310Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr343,407,41243,407,583
    nsv6715310RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr343,448,90443,449,075

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18676475duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18676475Submitted genomicNC_000003.12:g.434
    07412_43407583dup
    GRCh38 (hg38)NC_000003.12Chr343,407,41243,407,583
    nssv18676475RemappedPerfectNC_000003.11:g.434
    48904_43449075dup
    GRCh37.p13First PassNC_000003.11Chr343,448,90443,449,075

    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)
    nssv186764758e-062233792
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