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nsv6948072

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:129,960

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 572 SVs from 60 studies. See in: genome view    
    Submitted genomic42,780,820-42,910,779Question Mark
    Overlapping variant regions from other studies: 572 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):43,354,956-43,484,915Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6948072Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1342,780,82042,910,779
    nsv6948072RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1343,354,95643,484,915

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18604248duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18604248Submitted genomicNC_000013.11:g.427
    80820_42910779dup
    GRCh38 (hg38)NC_000013.11Chr1342,780,82042,910,779
    nssv18604248RemappedPerfectNC_000013.10:g.433
    54956_43484915dup
    GRCh37.p13First PassNC_000013.10Chr1343,354,95643,484,915

    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)
    nssv186042484e-061275652
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