A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636163



Internal ID6676272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36906795..37095249hg38UCSC Ensembl
chr15:37198996..37387450hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38188455
hg19188455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15217017, essv15217019, essv15217018
SamplesNA19324, HG00365, NA19328
Known GenesMEIS2, MIR8063
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636163
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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