A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617989



Internal ID6658184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90132496..90173531hg38UCSC Ensembl
chr8:91144724..91185759hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3841036
hg1941036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13253696
SamplesNA18971
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617989
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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