A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4969n100



Internal ID22791056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164258447..164376855hg38UCSC Ensembl
chr3:163976235..164094643hg19UCSC Ensembl
chr3:165458929..165577337hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38118409
hg19118409
hg18118409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007325, nsv1003471, nsv1008208
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)dgv4969n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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