U.S. flag

An official website of the United States government

nsv6912363

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:204

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 17 studies. See in: genome view    
    Submitted genomic74,174,037-74,174,240Question Mark
    Overlapping variant regions from other studies: 74 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):73,885,082-73,885,285Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912363Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,174,03774,174,240
    nsv6912363RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,885,08273,885,285

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18571710duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18571710Submitted genomicNC_000011.10:g.741
    74037_74174240dup
    GRCh38 (hg38)NC_000011.10Chr1174,174,03774,174,240
    nssv18571710RemappedPerfectNC_000011.9:g.7388
    5082_73885285dup
    GRCh37.p13First PassNC_000011.9Chr1173,885,08273,885,285

    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)
    nssv185717101.3e-053232784
    Support Center