A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637473



Internal ID7024265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100311230..100508356hg38UCSC Ensembl
chr15:100851435..101048561hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38197127
hg19197127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15350838, essv15350836, essv15350837, essv15350839
SamplesNA20861, HG03914, HG03991, HG04093
Known GenesADAMTS17, CERS3, SPATA41
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637473
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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