A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5414556



Internal ID9718402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43176583..43178127hg38UCSC Ensembl
chr15:43468781..43470325hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381545
hg191545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678276
Supporting Variants
SamplesNA19470
Known GenesTMEM62
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5414556
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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