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nsv6849045

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,174

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 20 studies. See in: genome view    
    Submitted genomic58,117,458-58,128,631Question Mark
    Overlapping variant regions from other studies: 115 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):59,030,017-59,041,190Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6849045Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr858,117,45858,128,631
    nsv6849045RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr859,030,01759,041,190

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744118duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744118Submitted genomicNC_000008.11:g.581
    17458_58128631dup
    GRCh38 (hg38)NC_000008.11Chr858,117,45858,128,631
    nssv18744118RemappedPerfectNC_000008.10:g.590
    30017_59041190dup
    GRCh37.p13First PassNC_000008.10Chr859,030,01759,041,190

    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)
    nssv187441184e-061276104
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