U.S. flag

An official website of the United States government

nsv6790413

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
    Submitted genomic148,463,101-148,466,600Question Mark
    Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):147,842,664-147,846,163Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6790413Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5148,463,101148,466,600
    nsv6790413RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5147,842,664147,846,163

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18506448deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18506448Submitted genomicNC_000005.10:g.148
    463101_148466600de
    l
    GRCh38 (hg38)NC_000005.10Chr5148,463,101148,466,600
    nssv18506448RemappedPerfectNC_000005.9:g.1478
    42664_147846163del
    GRCh37.p13First PassNC_000005.9Chr5147,842,664147,846,163

    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)
    nssv18506448<0.001126274676
    Support Center