A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616890



Internal ID7003776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35775698..35785609hg38UCSC Ensembl
Innerchr8:35775698..35785609hg38UCSC Ensembl
Outerchr8:35775427..35785893hg38UCSC Ensembl
chr8:35633216..35643127hg19UCSC Ensembl
Innerchr8:35633216..35643127hg19UCSC Ensembl
Outerchr8:35632945..35643411hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389912
hg199912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13167940
SamplesHG00475
Known GenesUNC5D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616890
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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