A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14028066



Internal ID6591716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10346392..10349280hg38UCSC Ensembl
Innerchr11:10346431..10349242hg38UCSC Ensembl
Outerchr11:10346354..10349319hg38UCSC Ensembl
chr11:10367939..10370827hg19UCSC Ensembl
Innerchr11:10367978..10370789hg19UCSC Ensembl
Outerchr11:10367901..10370866hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382889
hg192889
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625357
Supporting Variants
SamplesNA20768
Known GenesCAND1.11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14028066
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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