A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2693n100



Internal ID22788780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2593295..2676863hg38UCSC Ensembl
chr16:2643296..2726864hg19UCSC Ensembl
chr16:2583297..2666865hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3883569
hg1983569
hg1883569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043577, nsv1039187
Samples
Known GenesERVK13-1, FLJ42627, LOC652276, PDPK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2693n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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