A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6736n54



Internal ID22774631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24491300..24492157hg38UCSC Ensembl
chr2:24714169..24715026hg19UCSC Ensembl
chr2:24567673..24568530hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581198, nsv581197, nsv581196
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6736n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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