A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660950



Internal ID9927055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21722773..21727987hg38UCSC Ensembl
chr14:22191020..22196261hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385215
hg195242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5629279, essv6471543, essv6506386, essv6468640
SamplesNA11920, NA12275, HG01133, HG01334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660950
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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