A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3014n100



Internal ID22789101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70808194..71041712hg38UCSC Ensembl
chr16:70842097..71075615hg19UCSC Ensembl
chr16:69399598..69633116hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38233519
hg19233519
hg18233519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067305, nsv1057834
Samples
Known GenesHYDIN, HYDIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3014n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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