A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661049



Internal ID9927154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97663715..97674585hg38UCSC Ensembl
Outerchr14:97663678..97674635hg38UCSC Ensembl
Innerchr14:98130052..98140922hg19UCSC Ensembl
Outerchr14:98130015..98140972hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810958
hg1910958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5552750
SamplesNA19346
Known GenesLOC100129345
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661049
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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