U.S. flag

An official website of the United States government

nsv6773004

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,941,240

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6552 SVs from 106 studies. See in: genome view    
    Submitted genomic94,767,305-97,708,544Question Mark
    Overlapping variant regions from other studies: 6553 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):94,103,010-97,044,248Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6773004Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr594,767,30597,708,544
    nsv6773004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr594,103,01097,044,248

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18517308deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18517308Submitted genomicNC_000005.10:g.947
    67305_97708544del
    GRCh38 (hg38)NC_000005.10Chr594,767,30597,708,544
    nssv18517308RemappedPerfectNC_000005.9:g.9410
    3010_97044248del
    GRCh37.p13First PassNC_000005.9Chr594,103,01097,044,248

    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)
    nssv185173084e-061275920
    Support Center