A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617687



Internal ID7004572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75634008..75637271hg38UCSC Ensembl
Innerchr8:75634014..75637266hg38UCSC Ensembl
Outerchr8:75634003..75637277hg38UCSC Ensembl
chr8:76546243..76549506hg19UCSC Ensembl
Innerchr8:76546249..76549501hg19UCSC Ensembl
Outerchr8:76546238..76549512hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg383264
hg193264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13234741
SamplesHG01610
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617687
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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