U.S. flag

An official website of the United States government

nsv7043991

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,372,150

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4066 SVs from 110 studies. See in: genome view    
    Submitted genomic130,170,282-131,542,431Question Mark
    Overlapping variant regions from other studies: 4066 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):130,927,855-132,300,004Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043991Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2130,170,282131,542,431
    nsv7043991RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2130,927,855132,300,004

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765915inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765915Submitted genomicNC_000002.12:g.130
    170282_131542431in
    v
    GRCh38 (hg38)NC_000002.12Chr2130,170,282131,542,431
    nssv18765915RemappedPerfectNC_000002.11:g.130
    927855_132300004in
    v
    GRCh37.p13First PassNC_000002.11Chr2130,927,855132,300,004

    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)
    nssv187659157e-062276268
    Support Center