A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2967n100



Internal ID22789054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:35294244..35383152hg38UCSC Ensembl
chr16:34528615..34617523hg19UCSC Ensembl
chr16:34386116..34475024hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3888909
hg1988909
hg1888909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060794, nsv1057411
Samples
Known GenesLOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2967n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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