A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3430595



Internal ID15277551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22515887..22527685hg38UCSC Ensembl
Innerchr15:22516887..22526685hg38UCSC Ensembl
Outerchr15:22514887..22528685hg38UCSC Ensembl
chr15:23345411..23357209hg19UCSC Ensembl
Innerchr15:23346411..23356209hg19UCSC Ensembl
Outerchr15:23344411..23358209hg19UCSC Ensembl
chr15:20896852..20908650hg18UCSC Ensembl
Innerchr15:20897852..20907650hg18UCSC Ensembl
Outerchr15:20895852..20909650hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811799
hg1911799
hg1811799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689687
SamplesNA19240
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3430595
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer