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nsv6777665

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,691

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 26 studies. See in: genome view    
    Submitted genomic76,595,076-76,604,766Question Mark
    Overlapping variant regions from other studies: 143 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):75,890,901-75,900,591Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6777665Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr576,595,07676,604,766
    nsv6777665RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr575,890,90175,900,591

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18706960duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18706960Submitted genomicNC_000005.10:g.765
    95076_76604766dup
    GRCh38 (hg38)NC_000005.10Chr576,595,07676,604,766
    nssv18706960RemappedPerfectNC_000005.9:g.7589
    0901_75900591dup
    GRCh37.p13First PassNC_000005.9Chr575,890,90175,900,591

    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)
    nssv187069604e-061275894
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