U.S. flag

An official website of the United States government

nsv7006960

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 327 SVs from 46 studies. See in: genome view    
    Submitted genomic37,699,701-37,756,800Question Mark
    Overlapping variant regions from other studies: 323 SVs from 46 studies. See in: genome view    
    Remapped(Score: Good):38,190,602-38,247,440Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7006960Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1937,699,70137,756,800
    nsv7006960RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1938,190,60238,247,440

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423583deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423583Submitted genomicNC_000019.10:g.376
    99701_37756800del
    GRCh38 (hg38)NC_000019.10Chr1937,699,70137,756,800
    nssv18423583RemappedGoodNC_000019.9:g.3819
    0602_38247440del
    GRCh37.p13First PassNC_000019.9Chr1938,190,60238,247,440

    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)
    nssv184235831.9e-055253880
    Support Center