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nsv6786592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,393

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
    Submitted genomic56,982,640-57,007,032Question Mark
    Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):56,847,438-56,871,830Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6786592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr656,982,64057,007,032
    nsv6786592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr656,847,43856,871,830

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18526667deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18526667Submitted genomicNC_000006.12:g.569
    82640_57007032del
    GRCh38 (hg38)NC_000006.12Chr656,982,64057,007,032
    nssv18526667RemappedPerfectNC_000006.11:g.568
    47438_56871830del
    GRCh37.p13First PassNC_000006.11Chr656,847,43856,871,830

    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)
    nssv185266671.1e-053276204
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