A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6156275



Internal ID9133678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101923805..101923927hg38UCSC Ensembl
chr14:102390142..102390264hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2656703
Supporting Variants
SamplesNA19720
Known GenesPPP2R5C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6156275
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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