A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4641n100



Internal ID20156257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3934721..4221511hg38UCSC Ensembl
chr3:3976405..4263195hg19UCSC Ensembl
chr3:3951405..4238195hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38286791
hg19286791
hg18286791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998087, nsv1009265, nsv1008517, nsv997534, nsv1001115, nsv1010198
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)dgv4641n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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