A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626862



Internal ID7013692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75888624..75928589hg38UCSC Ensembl
Innerchr11:75888624..75928589hg38UCSC Ensembl
Outerchr11:75888124..75929089hg38UCSC Ensembl
chr11:75599668..75639633hg19UCSC Ensembl
Innerchr11:75599668..75639633hg19UCSC Ensembl
Outerchr11:75599168..75640133hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3839966
hg1939966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214075
SamplesNA20783
Known GenesUVRAG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626862
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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