A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639878



Internal ID6679968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8193720..8214825hg38UCSC Ensembl
Innerchr17:8194220..8214325hg38UCSC Ensembl
Outerchr17:8192720..8215825hg38UCSC Ensembl
chr17:8097038..8118143hg19UCSC Ensembl
Innerchr17:8097538..8117643hg19UCSC Ensembl
Outerchr17:8096038..8119143hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3821106
hg1921106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15605439
SamplesHG04225
Known GenesAURKB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639878
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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