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nsv6322181

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:483

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 20 studies. See in: genome view    
    Submitted genomic55,154,743-55,155,225Question Mark
    Overlapping variant regions from other studies: 109 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):55,620,416-55,620,898Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6322181Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr155,154,74355,155,225
    nsv6322181RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr155,620,41655,620,898

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18062204deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18062204Submitted genomicNC_000001.11:g.551
    54743_55155225del
    GRCh38 (hg38)NC_000001.11Chr155,154,74355,155,225
    nssv18062204RemappedPerfectNC_000001.10:g.556
    20416_55620898del
    GRCh37.p13First PassNC_000001.10Chr155,620,41655,620,898

    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)
    nssv180622040.0027237950
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