U.S. flag

An official website of the United States government

nsv6413715

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:446

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view    
    Submitted genomic83,654,543-83,654,988Question Mark
    Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):84,364,262-84,364,707Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6413715Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr683,654,54383,654,988
    nsv6413715RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr684,364,26284,364,707

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18145915deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18145915Submitted genomicNC_000006.12:g.836
    54543_83654988del
    GRCh38 (hg38)NC_000006.12Chr683,654,54383,654,988
    nssv18145915RemappedPerfectNC_000006.11:g.843
    64262_84364707del
    GRCh37.p13First PassNC_000006.11Chr684,364,26284,364,707

    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)
    nssv18145915<0.0012937302
    Support Center