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nsv6962360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,043

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 27 studies. See in: genome view    
    Submitted genomic92,484,855-92,494,897Question Mark
    Overlapping variant regions from other studies: 145 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):93,028,085-93,038,127Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1592,484,85592,494,897
    nsv6962360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1593,028,08593,038,127

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18397700deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18397700Submitted genomicNC_000015.10:g.924
    84855_92494897del
    GRCh38 (hg38)NC_000015.10Chr1592,484,85592,494,897
    nssv18397700RemappedPerfectNC_000015.9:g.9302
    8085_93038127del
    GRCh37.p13First PassNC_000015.9Chr1593,028,08593,038,127

    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)
    nssv183977004e-061276224
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