A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13358376



Internal ID1882409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141077577..141085707hg38UCSC Ensembl
Innerchr8:141077608..141085677hg38UCSC Ensembl
Outerchr8:141077547..141085738hg38UCSC Ensembl
chr8:142087676..142095806hg19UCSC Ensembl
Innerchr8:142087707..142095776hg19UCSC Ensembl
Outerchr8:142087646..142095837hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg388131
hg198131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619050
Supporting Variants
SamplesHG01775
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13358376
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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