A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4701n100



Internal ID22790788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23080476..23113674hg38UCSC Ensembl
chr3:23121967..23155165hg19UCSC Ensembl
chr3:23096971..23130169hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3833199
hg1933199
hg1833199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006921, nsv1010493
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)dgv4701n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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