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nsv6844343

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,527

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 17 studies. See in: genome view    
    Submitted genomic55,154,918-55,163,444Question Mark
    Overlapping variant regions from other studies: 110 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):56,067,478-56,076,004Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6844343Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr855,154,91855,163,444
    nsv6844343RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr856,067,47856,076,004

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18554243deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18554243Submitted genomicNC_000008.11:g.551
    54918_55163444del
    GRCh38 (hg38)NC_000008.11Chr855,154,91855,163,444
    nssv18554243RemappedPerfectNC_000008.10:g.560
    67478_56076004del
    GRCh37.p13First PassNC_000008.10Chr856,067,47856,076,004

    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)
    nssv185542434e-061276244
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