A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627056



Internal ID7013886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85057757..85067084hg38UCSC Ensembl
Innerchr11:85058257..85066584hg38UCSC Ensembl
Outerchr11:85056757..85068084hg38UCSC Ensembl
chr11:84768801..84778128hg19UCSC Ensembl
Innerchr11:84769301..84777628hg19UCSC Ensembl
Outerchr11:84767801..84779128hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg389328
hg199328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14221272, essv14221271
SamplesNA19058, HG02450
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627056
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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