A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617958



Internal ID7004841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88832027..88984631hg38UCSC Ensembl
chr8:89844256..89996860hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38152605
hg19152605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13251625
SamplesHG00566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617958
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer