U.S. flag

An official website of the United States government

nsv6613896

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,944

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 38 studies. See in: genome view    
    Submitted genomic45,730,517-45,741,460Question Mark
    Overlapping variant regions from other studies: 109 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):45,770,116-45,781,059Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6613896Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr745,730,51745,741,460
    nsv6613896RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr745,770,11645,781,059

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18155077deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18155077Submitted genomicNC_000007.14:g.457
    30517_45741460del
    GRCh38 (hg38)NC_000007.14Chr745,730,51745,741,460
    nssv18155077RemappedPerfectNC_000007.13:g.457
    70116_45781059del
    GRCh37.p13First PassNC_000007.13Chr745,770,11645,781,059

    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)
    nssv18155077<0.001139158
    Support Center