A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617957



Internal ID7004840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88756300..88849941hg38UCSC Ensembl
Innerchr8:88756300..88849941hg38UCSC Ensembl
Outerchr8:88755800..88850441hg38UCSC Ensembl
chr8:89768529..89862170hg19UCSC Ensembl
Innerchr8:89768529..89862170hg19UCSC Ensembl
Outerchr8:89768029..89862670hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3893642
hg1993642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13251624
SamplesHG00566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617957
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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