A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2969n100



Internal ID22789056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:35330247..35438659hg38UCSC Ensembl
chr16:34564618..34673030hg19UCSC Ensembl
chr16:34422119..34530531hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38108413
hg19108413
hg18108413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066944, nsv1060504, nsv1055973
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)dgv2969n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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