A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8378n54



Internal ID22776273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72732656..72735474hg38UCSC Ensembl
chr3:72781807..72784625hg19UCSC Ensembl
chr3:72864497..72867315hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382819
hg192819
hg182819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590630, nsv590629
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8378n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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