A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15266032



Internal ID5075747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62307996..62321068hg38UCSC Ensembl
chr15:62600195..62613267hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3813073
hg1913073
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636698
Supporting Variants
SamplesNA18542
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15266032
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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