A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636933



Internal ID7023727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75908231..76025938hg38UCSC Ensembl
chr15:76200572..76318279hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38117708
hg19117708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15293131
SamplesHG02816
Known GenesFBXO22, FBXO22-AS1, NRG4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636933
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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