U.S. flag

An official website of the United States government

nsv6677105

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:685

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 26 studies. See in: genome view    
    Submitted genomic228,696,005-228,696,689Question Mark
    Overlapping variant regions from other studies: 148 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):228,831,752-228,832,436Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6677105Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1228,696,005228,696,689
    nsv6677105RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1228,831,752228,832,436

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18368624deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18368624Submitted genomicNC_000001.11:g.228
    696005_228696689de
    l
    GRCh38 (hg38)NC_000001.11Chr1228,696,005228,696,689
    nssv18368624RemappedPerfectNC_000001.10:g.228
    831752_228832436de
    l
    GRCh37.p13First PassNC_000001.10Chr1228,831,752228,832,436

    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)
    nssv183686240.012487246332
    Support Center