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nsv6911748

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 365 SVs from 52 studies. See in: genome view    
    Submitted genomic6,314,301-6,441,800Question Mark
    Overlapping variant regions from other studies: 365 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):6,335,531-6,463,030Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6911748Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,314,3016,441,800
    nsv6911748RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,335,5316,463,030

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18352821deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18352821Submitted genomicNC_000011.10:g.631
    4301_6441800del
    GRCh38 (hg38)NC_000011.10Chr116,314,3016,441,800
    nssv18352821RemappedPerfectNC_000011.9:g.6335
    531_6463030del
    GRCh37.p13First PassNC_000011.9Chr116,335,5316,463,030

    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)
    nssv183528214e-061276218
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