A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13302955



Internal ID6583930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119136418..119142141hg38UCSC Ensembl
Innerchr8:119136418..119142141hg38UCSC Ensembl
Outerchr8:119135918..119142641hg38UCSC Ensembl
chr8:120148657..120154380hg19UCSC Ensembl
Innerchr8:120148657..120154380hg19UCSC Ensembl
Outerchr8:120148157..120154880hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg385724
hg195724
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3618589
Supporting Variants
SamplesNA20765
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13302955
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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