A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6152427



Internal ID9023467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25535839..25536862hg38UCSC Ensembl
Outerchr11:25535682..25537015hg38UCSC Ensembl
Innerchr11:25557385..25558408hg19UCSC Ensembl
Outerchr11:25557228..25558561hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660265
Supporting Variants
SamplesHG00650
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6152427
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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