A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618203



Internal ID7005086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101375349..101391559hg38UCSC Ensembl
Innerchr8:101375350..101391558hg38UCSC Ensembl
Outerchr8:101375348..101391560hg38UCSC Ensembl
chr8:102387577..102403787hg19UCSC Ensembl
Innerchr8:102387578..102403786hg19UCSC Ensembl
Outerchr8:102387576..102403788hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3816211
hg1916211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13269410, essv13269409, essv13269416, essv13269414, essv13269408, essv13269417, essv13269411, essv13269413, essv13269415, essv13269412
SamplesHG03091, HG03479, NA19456, NA18910, HG03563, NA20282, HG02759, NA20357, NA19117, NA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618203
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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