A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4832n100



Internal ID22790919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104363103..104560543hg38UCSC Ensembl
chr3:104081947..104279387hg19UCSC Ensembl
chr3:105564637..105762077hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38197441
hg19197441
hg18197441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998256, nsv997449
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)dgv4832n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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