A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3448284



Internal ID15295233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20487585..20493283hg38UCSC Ensembl
Innerchr15:20488585..20492283hg38UCSC Ensembl
Outerchr15:20486585..20494283hg38UCSC Ensembl
chr15:20692838..20698536hg19UCSC Ensembl
Innerchr15:20693838..20697536hg19UCSC Ensembl
Outerchr15:20691838..20699536hg19UCSC Ensembl
chr15:18952852..18958550hg18UCSC Ensembl
Innerchr15:18953852..18957550hg18UCSC Ensembl
Outerchr15:18951852..18959550hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg385699
hg195699
hg185699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689569
SamplesNA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3448284
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