A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2788n100



Internal ID22788875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19928432..19951789hg38UCSC Ensembl
chr16:19939754..19963111hg19UCSC Ensembl
chr16:19847255..19870612hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3823358
hg1923358
hg1823358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048745, nsv1037882
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)dgv2788n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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