A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14252421



Internal ID2686121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101879160..101881187hg38UCSC Ensembl
Innerchr11:101879176..101881171hg38UCSC Ensembl
Outerchr11:101879144..101881203hg38UCSC Ensembl
chr11:101749891..101751918hg19UCSC Ensembl
Innerchr11:101749907..101751902hg19UCSC Ensembl
Outerchr11:101749875..101751934hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382028
hg192028
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627517
Supporting Variants
SamplesHG02379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14252421
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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