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nsv6785744

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 41 studies. See in: genome view    
    Submitted genomic179,693,350-179,693,466Question Mark
    Overlapping variant regions from other studies: 127 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):179,120,351-179,120,467Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785744Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5179,693,350179,693,466
    nsv6785744RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,120,351179,120,467

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510932deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510932Submitted genomicNC_000005.10:g.179
    693350_179693466de
    l
    GRCh38 (hg38)NC_000005.10Chr5179,693,350179,693,466
    nssv18510932RemappedPerfectNC_000005.9:g.1791
    20351_179120467del
    GRCh37.p13First PassNC_000005.9Chr5179,120,351179,120,467

    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)
    nssv185109320.34791648260728
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