A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621201



Internal ID6661380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98068567..98407578hg38UCSC Ensembl
Innerchr9:98068717..98407428hg38UCSC Ensembl
Outerchr9:98068417..98407728hg38UCSC Ensembl
chr9:100830849..101169860hg19UCSC Ensembl
Innerchr9:100830999..101169710hg19UCSC Ensembl
Outerchr9:100830699..101170010hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38339012
hg19339012
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13574312
SamplesHG01602
Known GenesCORO2A, GABBR2, MIR6854, NANS, TBC1D2, TRIM14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621201
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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