A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667563



Internal ID9933668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155877000..155884580hg38UCSC Ensembl
chr2:156733512..156741092hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg387581
hg197581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5613585, essv6326394, essv5491615, essv5769480, essv6397334
SamplesNA19466, NA19396, NA07347, NA19395, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667563
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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