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nsv6847273

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,647

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 28 studies. See in: genome view    
    Submitted genomic39,159,644-39,187,290Question Mark
    Overlapping variant regions from other studies: 198 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):39,017,163-39,044,809Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6847273Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr839,159,64439,187,290
    nsv6847273RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr839,017,16339,044,809

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18554201deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18554201Submitted genomicNC_000008.11:g.391
    59644_39187290del
    GRCh38 (hg38)NC_000008.11Chr839,159,64439,187,290
    nssv18554201RemappedPerfectNC_000008.10:g.390
    17163_39044809del
    GRCh37.p13First PassNC_000008.10Chr839,017,16339,044,809

    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)
    nssv185542014e-061276158
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