A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13095659



Internal ID4459835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9447861..9455141hg38UCSC Ensembl
Innerchr8:9448011..9454991hg38UCSC Ensembl
Outerchr8:9447711..9455291hg38UCSC Ensembl
chr8:9305371..9312651hg19UCSC Ensembl
Innerchr8:9305521..9312501hg19UCSC Ensembl
Outerchr8:9305221..9312801hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg387281
hg197281
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616182
Supporting Variants
SamplesHG03967
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13095659
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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