A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4616n100



Internal ID20156232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:621944..1149322hg38UCSC Ensembl
chr3:663627..1191006hg19UCSC Ensembl
chr3:638627..1166006hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38527379
hg19527380
hg18527380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010757, nsv1007404
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4616n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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