A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4843n100



Internal ID22790930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117369686..117390341hg38UCSC Ensembl
chr3:117088533..117109188hg19UCSC Ensembl
chr3:118571223..118591878hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3820656
hg1920656
hg1820656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003873, nsv1009145
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)dgv4843n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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