A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628102



Internal ID7014927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131251482..131253827hg38UCSC Ensembl
Innerchr11:131251489..131253820hg38UCSC Ensembl
Outerchr11:131251475..131253834hg38UCSC Ensembl
chr11:131121377..131123722hg19UCSC Ensembl
Innerchr11:131121384..131123715hg19UCSC Ensembl
Outerchr11:131121370..131123729hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14314600, essv14314602, essv14314599, essv14314601
SamplesHG03652, NA20869, NA21123, HG03894
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628102
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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