A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3045n100



Internal ID22789132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80903546..80921496hg38UCSC Ensembl
chr16:80937443..80955393hg19UCSC Ensembl
chr16:79494944..79512894hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3817951
hg1917951
hg1817951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055556, nsv1065336, nsv1067522, nsv1058135, nsv1063397
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)dgv3045n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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