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nsv6525723

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,943

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 33 studies. See in: genome view    
    Submitted genomic58,077,107-58,083,049Question Mark
    Overlapping variant regions from other studies: 106 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):58,588,474-58,594,416Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6525723Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1958,077,10758,083,049
    nsv6525723RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,588,47458,594,416

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049034deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049034Submitted genomicNC_000019.10:g.580
    77107_58083049del
    GRCh38 (hg38)NC_000019.10Chr1958,077,10758,083,049
    nssv18049034RemappedPerfectNC_000019.9:g.5858
    8474_58594416del
    GRCh37.p13First PassNC_000019.9Chr1958,588,47458,594,416

    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)
    nssv18049034<0.001239112
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