A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627971



Internal ID7014796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124083868..124088412hg38UCSC Ensembl
Innerchr11:124083878..124088403hg38UCSC Ensembl
Outerchr11:124083859..124088422hg38UCSC Ensembl
chr11:123954575..123959119hg19UCSC Ensembl
Innerchr11:123954585..123959110hg19UCSC Ensembl
Outerchr11:123954566..123959129hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg384545
hg194545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14301613, essv14301615, essv14301614
SamplesNA20798, NA19658, HG01431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627971
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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