A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518639



Internal ID15445932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75083167..75108141hg38UCSC Ensembl
Innerchr10:76842925..76867899hg19UCSC Ensembl
Innerchr10:76512931..76537905hg18UCSC Ensembl
Innerchr10:76512931..76537905hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3824975
hg1924975
hg1824975
hg1724975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696088
Samples
Known GenesDUSP13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518639
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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