A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617184



Internal ID6657380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50817538..50971635hg38UCSC Ensembl
chr8:51730098..51884195hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38154098
hg19154098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13198146
SamplesNA18602
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617184
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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