A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15293131



Internal ID3212405
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636933
Supporting Variants
SamplesHG02816
Known GenesFBXO22, FBXO22-AS1, NRG4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15293131
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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