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nsv6965722

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 46 studies. See in: genome view    
    Submitted genomic5,056,101-5,061,400Question Mark
    Overlapping variant regions from other studies: 181 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):5,106,102-5,111,401Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6965722Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr165,056,1015,061,400
    nsv6965722RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr165,106,1025,111,401

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18401141deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18401141Submitted genomicNC_000016.10:g.505
    6101_5061400del
    GRCh38 (hg38)NC_000016.10Chr165,056,1015,061,400
    nssv18401141RemappedPerfectNC_000016.9:g.5106
    102_5111401del
    GRCh37.p13First PassNC_000016.9Chr165,106,1025,111,401

    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)
    nssv184011410.003900257996
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