A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15182029



Internal ID6563649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23786681..23953467hg38UCSC Ensembl
chr15:24031828..24198614hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38166787
hg19166787
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635850
Supporting Variants
SamplesNA20757
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15182029
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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