U.S. flag

An official website of the United States government

nsv6894552

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:197

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 22 studies. See in: genome view    
    Submitted genomic80,287,609-80,287,805Question Mark
    Overlapping variant regions from other studies: 127 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):82,047,365-82,047,561Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6894552Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1080,287,60980,287,805
    nsv6894552RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1082,047,36582,047,561

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18587796duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18587796Submitted genomicNC_000010.11:g.802
    87609_80287805dup
    GRCh38 (hg38)NC_000010.11Chr1080,287,60980,287,805
    nssv18587796RemappedPerfectNC_000010.10:g.820
    47365_82047561dup
    GRCh37.p13First PassNC_000010.10Chr1082,047,36582,047,561

    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)
    nssv185877964e-061236756
    Support Center