A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635990



Internal ID6676100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28108015..28121432hg38UCSC Ensembl
chr15:28353161..28366578hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3813418
hg1913418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15198897, essv15198895, essv15198896
SamplesNA18489, HG02143, HG03039
Known GenesHERC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635990
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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