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nsv6324604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:425

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 18 studies. See in: genome view    
    Submitted genomic84,862,564-84,862,988Question Mark
    Overlapping variant regions from other studies: 127 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):85,328,247-85,328,671Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6324604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr184,862,56484,862,988
    nsv6324604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr185,328,24785,328,671

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18064778deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18064778Submitted genomicNC_000001.11:g.848
    62564_84862988del
    GRCh38 (hg38)NC_000001.11Chr184,862,56484,862,988
    nssv18064778RemappedPerfectNC_000001.10:g.853
    28247_85328671del
    GRCh37.p13First PassNC_000001.10Chr185,328,24785,328,671

    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)
    nssv18064778<0.001134668
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