A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616612



Internal ID6656808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22534579..22537418hg38UCSC Ensembl
Innerchr8:22534593..22537404hg38UCSC Ensembl
Outerchr8:22534565..22537432hg38UCSC Ensembl
chr8:22392092..22394931hg19UCSC Ensembl
Innerchr8:22392106..22394917hg19UCSC Ensembl
Outerchr8:22392078..22394945hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382840
hg192840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13133491
SamplesHG03861
Known GenesPPP3CC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616612
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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