U.S. flag

An official website of the United States government

nsv7001048

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,724

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 37 studies. See in: genome view    
    Submitted genomic36,815,137-36,823,860Question Mark
    Overlapping variant regions from other studies: 168 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):37,306,039-37,314,762Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7001048Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,815,13736,823,860
    nsv7001048RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,306,03937,314,762

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423094deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423094Submitted genomicNC_000019.10:g.368
    15137_36823860del
    GRCh38 (hg38)NC_000019.10Chr1936,815,13736,823,860
    nssv18423094RemappedPerfectNC_000019.9:g.3730
    6039_37314762del
    GRCh37.p13First PassNC_000019.9Chr1937,306,03937,314,762

    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)
    nssv184230944e-061276254
    Support Center