A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661876



Internal ID9581295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32674959..32676063hg38UCSC Ensembl
Outerchr2:32674922..32676113hg38UCSC Ensembl
Innerchr2:32900026..32901130hg19UCSC Ensembl
Outerchr2:32899989..32901180hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6479948
SamplesNA18959
Known GenesTTC27
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661876
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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