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nsv6954947

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 25 studies. See in: genome view    
    Submitted genomic74,344,601-74,354,900Question Mark
    Overlapping variant regions from other studies: 168 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):74,918,738-74,929,037Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6954947Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1374,344,60174,354,900
    nsv6954947RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1374,918,73874,929,037

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18605956duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18605956Submitted genomicNC_000013.11:g.743
    44601_74354900dup
    GRCh38 (hg38)NC_000013.11Chr1374,344,60174,354,900
    nssv18605956RemappedPerfectNC_000013.10:g.749
    18738_74929037dup
    GRCh37.p13First PassNC_000013.10Chr1374,918,73874,929,037

    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)
    nssv186059564e-061274976
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