A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519956



Internal ID15447249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77800172..77842348hg38UCSC Ensembl
Innerchr2:78027298..78069474hg19UCSC Ensembl
Innerchr2:77880806..77922982hg18UCSC Ensembl
Innerchr2:77938953..77981129hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3842177
hg1942177
hg1842177
hg1742177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697145
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519956
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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