U.S. flag

An official website of the United States government

nsv6607568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:131

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 26 studies. See in: genome view    
    Submitted genomic44,221,430-44,221,560Question Mark
    Overlapping variant regions from other studies: 100 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):44,261,029-44,261,159Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6607568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr744,221,43044,221,560
    nsv6607568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr744,261,02944,261,159

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18154598deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18154598Submitted genomicNC_000007.14:g.442
    21430_44221560del
    GRCh38 (hg38)NC_000007.14Chr744,221,43044,221,560
    nssv18154598RemappedPerfectNC_000007.13:g.442
    61029_44261159del
    GRCh37.p13First PassNC_000007.13Chr744,261,02944,261,159

    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)
    nssv18154598<0.001126732
    Support Center