A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935772



Internal ID5418614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112224814..112226490hg38UCSC Ensembl
Innerchr10:112224814..112226490hg38UCSC Ensembl
Outerchr10:112224535..112226763hg38UCSC Ensembl
chr10:113984572..113986248hg19UCSC Ensembl
Innerchr10:113984572..113986248hg19UCSC Ensembl
Outerchr10:113984293..113986521hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624575
Supporting Variants
SamplesNA18950
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935772
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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