A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2991n100



Internal ID22789078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63250134..63367393hg38UCSC Ensembl
chr16:63284038..63401297hg19UCSC Ensembl
chr16:61841539..61958798hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38117260
hg19117260
hg18117260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055258, nsv1058736, nsv1055520, nsv1064724, nsv1059450
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2991n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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