A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6878n54



Internal ID22774773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52108526..52156194hg38UCSC Ensembl
chr2:52335664..52383332hg19UCSC Ensembl
chr2:52189168..52236836hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3847669
hg1947669
hg1847669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581924, nsv581925
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6878n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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