A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935595



Internal ID5969028
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624558
Supporting Variants
SamplesNA19379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935595
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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