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nsv6873542

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:536,965

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3028 SVs from 97 studies. See in: genome view    
    Submitted genomic144,315,680-144,852,644Question Mark
    Overlapping variant regions from other studies: 2380 SVs from 94 studies. See in: genome view    
    Remapped(Score: Pass):145,659,902-146,078,029Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6873542Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,315,680144,852,644
    nsv6873542RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,659,902146,078,029

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18553235deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18553235Submitted genomicNC_000008.11:g.144
    315680_144852644de
    l
    GRCh38 (hg38)NC_000008.11Chr8144,315,680144,852,644
    nssv18553235RemappedPassNC_000008.10:g.145
    659902_146078029de
    l
    GRCh37.p13First PassNC_000008.10Chr8145,659,902146,078,029

    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)
    nssv185532354e-061275290
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