A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13745155



Internal ID5184218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29863769..29868636hg38UCSC Ensembl
Innerchr10:29863832..29868574hg38UCSC Ensembl
Outerchr10:29863707..29868699hg38UCSC Ensembl
chr10:30152698..30157565hg19UCSC Ensembl
Innerchr10:30152761..30157503hg19UCSC Ensembl
Outerchr10:30152636..30157628hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384868
hg194868
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622781
Supporting Variants
SamplesNA18608
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13745155
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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