A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5949600



Internal ID9725128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61496854..61517326hg38UCSC Ensembl
chr14:61963572..61984044hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3820473
hg1920473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663429
Supporting Variants
SamplesNA19625
Known GenesPRKCH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5949600
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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