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nsv6908888

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,385

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 26 studies. See in: genome view    
    Submitted genomic63,644,944-63,653,328Question Mark
    Overlapping variant regions from other studies: 87 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):63,412,416-63,420,800Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908888Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1163,644,94463,653,328
    nsv6908888RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1163,412,41663,420,800

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351300deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351300Submitted genomicNC_000011.10:g.636
    44944_63653328del
    GRCh38 (hg38)NC_000011.10Chr1163,644,94463,653,328
    nssv18351300RemappedPerfectNC_000011.9:g.6341
    2416_63420800del
    GRCh37.p13First PassNC_000011.9Chr1163,412,41663,420,800

    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)
    nssv183513004e-061276260
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