A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616827



Internal ID7003713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33211448..33216655hg38UCSC Ensembl
Innerchr8:33211450..33216654hg38UCSC Ensembl
Outerchr8:33211447..33216657hg38UCSC Ensembl
chr8:33068966..33074173hg19UCSC Ensembl
Innerchr8:33068968..33074172hg19UCSC Ensembl
Outerchr8:33068965..33074175hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385208
hg195208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13160901, essv13160904, essv13160902, essv13160906, essv13160905, essv13160903
SamplesHG03105, HG02819, HG01286, HG02771, HG01912, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616827
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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