A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626888



Internal ID7013718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77610862..77622595hg38UCSC Ensembl
Innerchr11:77610862..77622595hg38UCSC Ensembl
Outerchr11:77610362..77623095hg38UCSC Ensembl
chr11:77321907..77333640hg19UCSC Ensembl
Innerchr11:77321907..77333640hg19UCSC Ensembl
Outerchr11:77321407..77334140hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811734
hg1911734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214979
SamplesHG02775
Known GenesCLNS1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626888
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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