U.S. flag

An official website of the United States government

nsv6908330

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49,622

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 176 SVs from 33 studies. See in: genome view    
    Submitted genomic57,265,656-57,315,277Question Mark
    Overlapping variant regions from other studies: 176 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):57,033,130-57,082,751Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908330Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1157,265,65657,315,277
    nsv6908330RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1157,033,13057,082,751

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351480deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351480Submitted genomicNC_000011.10:g.572
    65656_57315277del
    GRCh38 (hg38)NC_000011.10Chr1157,265,65657,315,277
    nssv18351480RemappedPerfectNC_000011.9:g.5703
    3130_57082751del
    GRCh37.p13First PassNC_000011.9Chr1157,033,13057,082,751

    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)
    nssv183514804e-061276168
    Support Center