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nsv6938835

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 24 studies. See in: genome view    
    Submitted genomic51,983,184-51,983,202Question Mark
    Overlapping variant regions from other studies: 174 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):52,557,320-52,557,338Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6938835Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1351,983,18451,983,202
    nsv6938835RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,557,32052,557,338

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18378420deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18378420Submitted genomicNC_000013.11:g.519
    83184_51983202del
    GRCh38 (hg38)NC_000013.11Chr1351,983,18451,983,202
    nssv18378420RemappedPerfectNC_000013.10:g.525
    57320_52557338del
    GRCh37.p13First PassNC_000013.10Chr1352,557,32052,557,338

    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)
    nssv18378420<0.00126248060
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