A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5842889



Internal ID9598794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46060331..46061219hg38UCSC Ensembl
chr13:46634466..46635354hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675321
Supporting Variants
SamplesNA19235
Known GenesCPB2, CPB2-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5842889
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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