U.S. flag

An official website of the United States government

nsv6895870

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
    Submitted genomic35,487,901-35,502,000Question Mark
    Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):35,776,829-35,790,928Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6895870Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1035,487,90135,502,000
    nsv6895870RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1035,776,82935,790,928

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18573224duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18573224Submitted genomicNC_000010.11:g.354
    87901_35502000dup
    GRCh38 (hg38)NC_000010.11Chr1035,487,90135,502,000
    nssv18573224RemappedPerfectNC_000010.10:g.357
    76829_35790928dup
    GRCh37.p13First PassNC_000010.10Chr1035,776,82935,790,928

    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)
    nssv185732244e-061274770
    Support Center