A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13251625



Internal ID943986
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3617958
Supporting Variants
SamplesHG00566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13251625
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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