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nsv7038651

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:170,975

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 671 SVs from 75 studies. See in: genome view    
    Submitted genomic56,300,383-56,471,357Question Mark
    Overlapping variant regions from other studies: 671 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):56,368,076-56,539,050Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038651Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr756,300,38356,471,357
    nsv7038651RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr756,368,07656,539,050

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780990inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780990Submitted genomicNC_000007.14:g.563
    00383_56471357inv
    GRCh38 (hg38)NC_000007.14Chr756,300,38356,471,357
    nssv18780990RemappedPerfectNC_000007.13:g.563
    68076_56539050inv
    GRCh37.p13First PassNC_000007.13Chr756,368,07656,539,050

    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)
    nssv187809907e-060276268
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