A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4926n100



Internal ID20156542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155757649..155797695hg38UCSC Ensembl
chr3:155475438..155515484hg19UCSC Ensembl
chr3:156958132..156998178hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3840047
hg1940047
hg1840047
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001756, nsv1006439, nsv1009635, nsv1007915
Samples
Known GenesC3orf33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4926n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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