A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1376e59



Internal ID22762596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22552987..22559185hg38UCSC Ensembl
chr15:23313911..23320109hg19UCSC Ensembl
chr15:20865352..20871550hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386199
hg196199
hg186199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3385626, esv3352262
SamplesNA19238, NA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1376e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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