A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621113



Internal ID6661293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94207958..94890837hg38UCSC Ensembl
Innerchr9:94208108..94890687hg38UCSC Ensembl
Outerchr9:94207808..94890987hg38UCSC Ensembl
chr9:96970240..97653119hg19UCSC Ensembl
Innerchr9:96970390..97652969hg19UCSC Ensembl
Outerchr9:96970090..97653269hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38682880
hg19682880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13567289
SamplesHG01602
Known GenesC9orf3, FBP1, FBP2, HIATL1, LOC100132077, MIR2278, NUTM2F, ZNF169
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621113
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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