A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13824672



Internal ID5838756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56816248..56856985hg38UCSC Ensembl
Innerchr10:56816257..56856977hg38UCSC Ensembl
Outerchr10:56816240..56856994hg38UCSC Ensembl
chr10:58576008..58616745hg19UCSC Ensembl
Innerchr10:58576017..58616737hg19UCSC Ensembl
Outerchr10:58576000..58616754hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3840738
hg1940738
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623399
Supporting Variants
SamplesNA19210
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13824672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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