A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4980n100



Internal ID22791067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166062138..166226838hg38UCSC Ensembl
chr3:165779926..165944626hg19UCSC Ensembl
chr3:167262620..167427320hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38164701
hg19164701
hg18164701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004611, nsv999621
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)dgv4980n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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