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nsv6339361

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,798

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 216 SVs from 56 studies. See in: genome view    
    Submitted genomic88,012,321-88,029,118Question Mark
    Overlapping variant regions from other studies: 218 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):88,311,840-88,328,637Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6339361Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr288,012,32188,029,118
    nsv6339361RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr288,311,84088,328,637

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18091800deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18091800Submitted genomicNC_000002.12:g.880
    12321_88029118del
    GRCh38 (hg38)NC_000002.12Chr288,012,32188,029,118
    nssv18091800RemappedPerfectNC_000002.11:g.883
    11840_88328637del
    GRCh37.p13First PassNC_000002.11Chr288,311,84088,328,637

    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)
    nssv18091800<0.001139196
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