A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13160897



Internal ID2580234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33179109..33180632hg38UCSC Ensembl
Innerchr8:33179115..33180626hg38UCSC Ensembl
Outerchr8:33179103..33180638hg38UCSC Ensembl
chr8:33036627..33038150hg19UCSC Ensembl
Innerchr8:33036633..33038144hg19UCSC Ensembl
Outerchr8:33036621..33038156hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616826
Supporting Variants
SamplesHG02284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13160897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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