A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631464



Internal ID7018273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21468952..21493635hg38UCSC Ensembl
chr13:22043091..22067774hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3824684
hg1924684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14662821
SamplesHG03741
Known GenesMICU2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631464
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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