A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618036



Internal ID7004919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92231845..92257304hg38UCSC Ensembl
Innerchr8:92231888..92257261hg38UCSC Ensembl
Outerchr8:92231802..92257347hg38UCSC Ensembl
chr8:93244073..93269532hg19UCSC Ensembl
Innerchr8:93244116..93269489hg19UCSC Ensembl
Outerchr8:93244030..93269575hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3825460
hg1925460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13257897
SamplesHG04202
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618036
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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