A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2834n100



Internal ID22788921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31948041..32197459hg38UCSC Ensembl
chr16:31959362..32208780hg19UCSC Ensembl
chr16:31866863..32116281hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38249419
hg19249419
hg18249419
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056441, nsv1055504
Samples
Known GenesHERC2P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2834n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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