A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665953



Internal ID9932058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14381791..14426909hg38UCSC Ensembl
Outerchr2:14381754..14426959hg38UCSC Ensembl
Innerchr2:14521915..14567033hg19UCSC Ensembl
Outerchr2:14521878..14567083hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3845206
hg1945206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6530823
SamplesNA20790
Known GenesLINC00276
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665953
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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