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nsv6942364

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 156 SVs from 22 studies. See in: genome view    
    Submitted genomic95,542,101-95,545,700Question Mark
    Overlapping variant regions from other studies: 156 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):96,194,355-96,197,954Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6942364Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1395,542,10195,545,700
    nsv6942364RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1396,194,35596,197,954

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18382790deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18382790Submitted genomicNC_000013.11:g.955
    42101_95545700del
    GRCh38 (hg38)NC_000013.11Chr1395,542,10195,545,700
    nssv18382790RemappedPerfectNC_000013.10:g.961
    94355_96197954del
    GRCh37.p13First PassNC_000013.10Chr1396,194,35596,197,954

    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)
    nssv183827903.9e-0511275396
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