A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2725n100



Internal ID20154341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8884313..9125030hg38UCSC Ensembl
chr16:8978170..9218887hg19UCSC Ensembl
chr16:8885671..9126388hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38240718
hg19240718
hg18240718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037383, nsv1042684, nsv1049081
Samples
Known GenesC16orf72, USP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2725n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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