U.S. flag

An official website of the United States government

nsv6532892

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 34 studies. See in: genome view    
    Submitted genomic57,194,301-57,203,000Question Mark
    Overlapping variant regions from other studies: 98 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):57,705,669-57,714,368Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6532892Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1957,194,30157,203,000
    nsv6532892RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1957,705,66957,714,368

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18048566deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18048566Submitted genomicNC_000019.10:g.571
    94301_57203000del
    GRCh38 (hg38)NC_000019.10Chr1957,194,30157,203,000
    nssv18048566RemappedPerfectNC_000019.9:g.5770
    5669_57714368del
    GRCh37.p13First PassNC_000019.9Chr1957,705,66957,714,368

    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)
    nssv180485660.00726939264
    Support Center