A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626068



Internal ID7012902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40535881..40590353hg38UCSC Ensembl
Innerchr11:40535881..40590353hg38UCSC Ensembl
Outerchr11:40535381..40590853hg38UCSC Ensembl
chr11:40557431..40611903hg19UCSC Ensembl
Innerchr11:40557431..40611903hg19UCSC Ensembl
Outerchr11:40556931..40612403hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3854473
hg1954473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14104446
SamplesNA20758
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626068
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer