A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625357



Internal ID7012191
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14028066
SamplesNA20768
Known GenesCAND1.11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625357
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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