A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8485n54



Internal ID22776380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103378433..103461553hg38UCSC Ensembl
chr3:103097277..103180397hg19UCSC Ensembl
chr3:104579967..104663087hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3883121
hg1983121
hg1883121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591195, nsv591198
Samples1780854599_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8485n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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