A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4762n100



Internal ID22790849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65200174..65237719hg38UCSC Ensembl
chr3:65185849..65223394hg19UCSC Ensembl
chr3:65160889..65198434hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3837546
hg1937546
hg1837546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999834, nsv998683, nsv997805, nsv1006125, nsv1013444, nsv997811, nsv1014849, nsv1014521, nsv1004636, nsv1011645
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)dgv4762n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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