A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663482



Internal ID9929587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102640550..102643697hg38UCSC Ensembl
Outerchr14:102640513..102643747hg38UCSC Ensembl
Innerchr14:103106887..103110034hg19UCSC Ensembl
Outerchr14:103106850..103110084hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg383235
hg193235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5840183
SamplesNA18916
Known GenesRCOR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663482
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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