A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6691n54



Internal ID22774586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10010802..10016433hg38UCSC Ensembl
chr2:10150929..10156560hg19UCSC Ensembl
chr2:10068380..10074011hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385632
hg195632
hg185632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580962, nsv580961
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6691n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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