A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14030828



Internal ID2519062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11814166..11822504hg38UCSC Ensembl
Innerchr11:11814166..11822504hg38UCSC Ensembl
Outerchr11:11813666..11823004hg38UCSC Ensembl
chr11:11835713..11844051hg19UCSC Ensembl
Innerchr11:11835713..11844051hg19UCSC Ensembl
Outerchr11:11835213..11844551hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg388339
hg198339
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625380
Supporting Variants
SamplesHG02235
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14030828
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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