A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3832n100



Internal ID22789919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52527318..52591653hg38UCSC Ensembl
chr2:52754456..52818791hg19UCSC Ensembl
chr2:52607960..52672295hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3864336
hg1964336
hg1864336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006118, nsv1012649, nsv1001243, nsv1013799, nsv1010707, nsv1004771
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3832n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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