A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624558



Internal ID7011411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111409067..111471819hg38UCSC Ensembl
Innerchr10:111409567..111471319hg38UCSC Ensembl
Outerchr10:111408067..111472819hg38UCSC Ensembl
chr10:113168825..113231577hg19UCSC Ensembl
Innerchr10:113169325..113231077hg19UCSC Ensembl
Outerchr10:113167825..113232577hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3862753
hg1962753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv166e214
Supporting Variantsessv13935595
SamplesNA19379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624558
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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