A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13946643



Internal ID3088052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118465594..118466839hg38UCSC Ensembl
Innerchr10:118465594..118466839hg38UCSC Ensembl
Outerchr10:118465073..118467114hg38UCSC Ensembl
chr10:120225106..120226351hg19UCSC Ensembl
Innerchr10:120225106..120226351hg19UCSC Ensembl
Outerchr10:120224585..120226626hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624691
Supporting Variants
SamplesHG02715
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13946643
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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