A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627210



Internal ID7014040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90556723..90639405hg38UCSC Ensembl
Innerchr11:90556738..90639390hg38UCSC Ensembl
Outerchr11:90556708..90639420hg38UCSC Ensembl
chr11:90289891..90372573hg19UCSC Ensembl
Innerchr11:90289906..90372558hg19UCSC Ensembl
Outerchr11:90289876..90372588hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3882683
hg1982683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14232098
SamplesHG01986
Known GenesDISC1FP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627210
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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