A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6918n54



Internal ID22774813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71115426..71120629hg38UCSC Ensembl
chr2:71342556..71347759hg19UCSC Ensembl
chr2:71196064..71201267hg18UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg385204
hg195204
hg185204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582195, nsv582194, nsv582196
Samples
Known GenesMCEE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6918n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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