U.S. flag

An official website of the United States government

nsv6529265

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:557,734

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2119 SVs from 92 studies. See in: genome view    
    Submitted genomic78,919,705-79,477,438Question Mark
    Overlapping variant regions from other studies: 1960 SVs from 91 studies. See in: genome view    
    Remapped(Score: Pass):76,915,787-77,412,076Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6529265Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1778,919,70579,477,438
    nsv6529265RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1776,915,78777,412,076

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18184112duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18184112Submitted genomicNC_000017.11:g.789
    19705_79477438dup
    GRCh38 (hg38)NC_000017.11Chr1778,919,70579,477,438
    nssv18184112RemappedPassNC_000017.10:g.769
    15787_77412076dup
    GRCh37.p13First PassNC_000017.10Chr1776,915,78777,412,076

    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)
    nssv18184112<0.001139244
    Support Center