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nsv6714570

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,707

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 24 studies. See in: genome view    
    Submitted genomic56,782,554-56,792,260Question Mark
    Overlapping variant regions from other studies: 97 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):56,816,582-56,826,288Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6714570Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr356,782,55456,792,260
    nsv6714570RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr356,816,58256,826,288

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18480857deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18480857Submitted genomicNC_000003.12:g.567
    82554_56792260del
    GRCh38 (hg38)NC_000003.12Chr356,782,55456,792,260
    nssv18480857RemappedPerfectNC_000003.11:g.568
    16582_56826288del
    GRCh37.p13First PassNC_000003.11Chr356,816,58256,826,288

    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)
    nssv184808571.8e-055275634
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