A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13169136



Internal ID3421134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38158909..38159796hg38UCSC Ensembl
Innerchr8:38158951..38159755hg38UCSC Ensembl
Outerchr8:38158868..38159838hg38UCSC Ensembl
chr8:38016427..38017314hg19UCSC Ensembl
Innerchr8:38016469..38017273hg19UCSC Ensembl
Outerchr8:38016386..38017356hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616919
Supporting Variants
SamplesHG03060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13169136
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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