A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2961n100



Internal ID22789048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34962968..35257961hg38UCSC Ensembl
chr16:34197339..34492332hg19UCSC Ensembl
chr16:34054840..34349833hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38294994
hg19294994
hg18294994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063819, nsv1064842
Samples
Known GenesUBE2MP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2961n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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