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nsv6612285

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,748

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 179 SVs from 44 studies. See in: genome view    
    Submitted genomic75,032,829-75,041,576Question Mark
    Overlapping variant regions from other studies: 73 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):2,562,065-2,570,812Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6612285Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr775,032,82975,041,576
    nsv6612285RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871064.1Chr7|NW_00
    3871064.1
    2,562,0652,570,812

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18159569deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18159569Submitted genomicNC_000007.14:g.750
    32829_75041576del
    GRCh38 (hg38)NC_000007.14Chr775,032,82975,041,576
    nssv18159569RemappedPerfectNW_003871064.1:g.2
    562065_2570812del
    GRCh37.p13First PassNW_003871064.1Chr7|NW_00
    3871064.1
    2,562,0652,570,812

    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)
    nssv18159569<0.001539170
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