U.S. flag

An official website of the United States government

nsv6504374

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:556

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 29 studies. See in: genome view    
    Submitted genomic31,888,144-31,888,699Question Mark
    Overlapping variant regions from other studies: 87 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):31,899,465-31,900,020Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6504374Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1631,888,14431,888,699
    nsv6504374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1631,899,46531,900,020

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18028986deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18028986Submitted genomicNC_000016.10:g.318
    88144_31888699del
    GRCh38 (hg38)NC_000016.10Chr1631,888,14431,888,699
    nssv18028986RemappedPerfectNC_000016.9:g.3189
    9465_31900020del
    GRCh37.p13First PassNC_000016.9Chr1631,899,46531,900,020

    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)
    nssv18028986<0.0012338602
    Support Center