A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3031n100



Internal ID20154647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77892138..78561070hg38UCSC Ensembl
chr16:77926035..78594967hg19UCSC Ensembl
chr16:76483536..77152468hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38668933
hg19668933
hg18668933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055930, nsv1064759
Samples
Known GenesCLEC3A, VAT1L, WWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3031n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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