A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620954



Internal ID7007824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86206746..86229458hg38UCSC Ensembl
chr9:88821661..88844373hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3822713
hg1922713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13544299, essv13544298, essv13544300
SamplesHG02356, NA18982, HG03594
Known GenesC9orf153
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620954
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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