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nsv6796824

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,385

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Submitted genomic170,530,804-170,539,188Question Mark
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):169,957,808-169,966,192Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6796824Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5170,530,804170,539,188
    nsv6796824RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5169,957,808169,966,192

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510552deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510552Submitted genomicNC_000005.10:g.170
    530804_170539188de
    l
    GRCh38 (hg38)NC_000005.10Chr5170,530,804170,539,188
    nssv18510552RemappedPerfectNC_000005.9:g.1699
    57808_169966192del
    GRCh37.p13First PassNC_000005.9Chr5169,957,808169,966,192

    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)
    nssv185105527e-062276158
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