A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2855n100



Internal ID22788942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32169453..32481160hg38UCSC Ensembl
chr16:32180774..32492481hg19UCSC Ensembl
chr16:32088275..32399982hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38311708
hg19311708
hg18311708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055543, nsv1066550, nsv1056893, nsv1061921, nsv1066385
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2855n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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