A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14025038



Internal ID5080536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9615649..9617547hg38UCSC Ensembl
Innerchr11:9615649..9617547hg38UCSC Ensembl
Outerchr11:9615373..9617809hg38UCSC Ensembl
chr11:9637196..9639094hg19UCSC Ensembl
Innerchr11:9637196..9639094hg19UCSC Ensembl
Outerchr11:9636920..9639356hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625339
Supporting Variants
SamplesNA18544
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14025038
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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