A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617501



Internal ID7004386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67384704..67398372hg38UCSC Ensembl
Innerchr8:67385204..67397872hg38UCSC Ensembl
Outerchr8:67383704..67399372hg38UCSC Ensembl
chr8:68296939..68310607hg19UCSC Ensembl
Innerchr8:68297439..68310107hg19UCSC Ensembl
Outerchr8:68295939..68311607hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3813669
hg1913669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13216293
SamplesNA20877
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617501
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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