A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2994n100



Internal ID22789081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65327036..65450341hg38UCSC Ensembl
chr16:65360939..65484244hg19UCSC Ensembl
chr16:63918440..64041745hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38123306
hg19123306
hg18123306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059013, nsv1057264, nsv1063041
Samples
Known GenesLINC00922
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2994n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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