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nsv6933297

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:399,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1178 SVs from 77 studies. See in: genome view    
    Submitted genomic57,414,401-57,814,000Question Mark
    Overlapping variant regions from other studies: 1178 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):57,808,184-58,207,783Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6933297Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1257,414,40157,814,000
    nsv6933297RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1257,808,18458,207,783

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18596017duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18596017Submitted genomicNC_000012.12:g.574
    14401_57814000dup
    GRCh38 (hg38)NC_000012.12Chr1257,414,40157,814,000
    nssv18596017RemappedPerfectNC_000012.11:g.578
    08184_58207783dup
    GRCh37.p13First PassNC_000012.11Chr1257,808,18458,207,783

    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)
    nssv185960173.7e-0510265318
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