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nsv6527146

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,219

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 23 studies. See in: genome view    
    Submitted genomic48,934,818-48,938,036Question Mark
    Overlapping variant regions from other studies: 143 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):47,012,180-47,015,398Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6527146Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1748,934,81848,938,036
    nsv6527146RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1747,012,18047,015,398

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18036088deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18036088Submitted genomicNC_000017.11:g.489
    34818_48938036del
    GRCh38 (hg38)NC_000017.11Chr1748,934,81848,938,036
    nssv18036088RemappedPerfectNC_000017.10:g.470
    12180_47015398del
    GRCh37.p13First PassNC_000017.10Chr1747,012,18047,015,398

    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)
    nssv18036088<0.001238978
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