A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618234



Internal ID7005117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102706138..102716175hg38UCSC Ensembl
Innerchr8:102706162..102716152hg38UCSC Ensembl
Outerchr8:102706115..102716199hg38UCSC Ensembl
chr8:103718366..103728403hg19UCSC Ensembl
Innerchr8:103718390..103728380hg19UCSC Ensembl
Outerchr8:103718343..103728427hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3810038
hg1910038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13270993, essv13270992
SamplesNA20507, NA20533
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618234
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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