U.S. flag

An official website of the United States government

nsv6888604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,675

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view    
    Submitted genomic69,264,254-69,277,928Question Mark
    Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):71,024,010-71,037,684Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6888604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1069,264,25469,277,928
    nsv6888604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1071,024,01071,037,684

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586733duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586733Submitted genomicNC_000010.11:g.692
    64254_69277928dup
    GRCh38 (hg38)NC_000010.11Chr1069,264,25469,277,928
    nssv18586733RemappedPerfectNC_000010.10:g.710
    24010_71037684dup
    GRCh37.p13First PassNC_000010.10Chr1071,024,01071,037,684

    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)
    nssv185867338.5e-0523275720
    Support Center