A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8805n54



Internal ID22776700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192671511..192674211hg38UCSC Ensembl
chr3:192389300..192392000hg19UCSC Ensembl
chr3:193871994..193874694hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382701
hg192701
hg182701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592885, nsv592884, nsv592888, nsv592887
Samples
Known GenesFGF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8805n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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