A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4720n100



Internal ID22790807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36580172..36646100hg38UCSC Ensembl
chr3:36621664..36687592hg19UCSC Ensembl
chr3:36596668..36662596hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3865929
hg1965929
hg1865929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009113, nsv998084, nsv997902, nsv1005535
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)dgv4720n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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