A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13544298



Internal ID2663229
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620954
Supporting Variants
SamplesHG02356
Known GenesC9orf153
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13544298
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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