A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4604n100



Internal ID22790691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..86250hg38UCSC Ensembl
chr3:60333..127933hg19UCSC Ensembl
chr3:35333..102933hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3867596
hg1967601
hg1867601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008330, nsv1010627, nsv1007799, nsv1000608
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)dgv4604n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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