A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616628



Internal ID6656824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23147893..23149030hg38UCSC Ensembl
Innerchr8:23147943..23148981hg38UCSC Ensembl
Outerchr8:23147844..23149080hg38UCSC Ensembl
chr8:23005406..23006543hg19UCSC Ensembl
Innerchr8:23005456..23006494hg19UCSC Ensembl
Outerchr8:23005357..23006593hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13134671, essv13134679, essv13134674, essv13134676, essv13134673, essv13134672, essv13134680, essv13134678, essv13134675, essv13134670, essv13134669, essv13134677
SamplesHG03706, HG02736, NA20906, HG02792, HG02143, NA20884, HG01271, HG03713, HG03943, NA20525, NA19747, HG03809
Known GenesTNFRSF10D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616628
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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