A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5915425



Internal ID9513381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12550018..12554945hg38UCSC Ensembl
chr19:12660832..12665759hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384928
hg194928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657782
Supporting Variants
SamplesNA18999
Known GenesZNF564
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5915425
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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