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nsv6546624

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:429

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 76 SVs from 17 studies. See in: genome view    
    Submitted genomic26,542,004-26,542,432Question Mark
    Overlapping variant regions from other studies: 76 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):26,937,970-26,938,398Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6546624Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2226,542,00426,542,432
    nsv6546624RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2226,937,97026,938,398

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18073171deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18073171Submitted genomicNC_000022.11:g.265
    42004_26542432del
    GRCh38 (hg38)NC_000022.11Chr2226,542,00426,542,432
    nssv18073171RemappedPerfectNC_000022.10:g.269
    37970_26938398del
    GRCh37.p13First PassNC_000022.10Chr2226,937,97026,938,398

    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)
    nssv18073171<0.001133376
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