A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8613n54



Internal ID22776508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136302210..136307259hg38UCSC Ensembl
chr3:136021052..136026101hg19UCSC Ensembl
chr3:137503742..137508791hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385050
hg195050
hg185050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591841, nsv591845, nsv591837, nsv591843, nsv591838, nsv591839, nsv591842, nsv591836, nsv591844
Samples
Known GenesPCCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8613n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss373
Observed Complex0
Frequencyn/a


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