A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637525



Internal ID6677629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101791620..101855327hg38UCSC Ensembl
chr15:102331823..102395530hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3863708
hg1963708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15354538, essv15354534, essv15354536, essv15354537, essv15354539, essv15354535
SamplesHG00121, HG01247, HG01762, HG00353, NA20797, NA12006
Known GenesOR4F13P, OR4F15, OR4F6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637525
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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