A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665034



Internal ID9931139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98711763..98727446hg38UCSC Ensembl
chr14:99178100..99193783hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3815684
hg1915684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5553295, essv6349739, essv5915778
SamplesHG01066, NA20811, HG00250
Known GenesC14orf177
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665034
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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