U.S. flag

An official website of the United States government

nsv6777946

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 17 studies. See in: genome view    
    Submitted genomic93,864,580-93,864,615Question Mark
    Overlapping variant regions from other studies: 114 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):93,200,286-93,200,321Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6777946Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr593,864,58093,864,615
    nsv6777946RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr593,200,28693,200,321

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18517210deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18517210Submitted genomicNC_000005.10:g.938
    64580_93864615del
    GRCh38 (hg38)NC_000005.10Chr593,864,58093,864,615
    nssv18517210RemappedPerfectNC_000005.9:g.9320
    0286_93200321del
    GRCh37.p13First PassNC_000005.9Chr593,200,28693,200,321

    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)
    nssv18517210<0.00181251872
    Support Center