A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659162



Internal ID9925267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95976143..95983151hg38UCSC Ensembl
Outerchr14:95976106..95983201hg38UCSC Ensembl
Innerchr14:96442480..96449488hg19UCSC Ensembl
Outerchr14:96442443..96449538hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387096
hg197096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5811180
SamplesNA18612
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659162
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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