A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13373813



Internal ID4426496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:148486..193583hg38UCSC Ensembl
chr9:148486..193583hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3845098
hg1945098
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619171
Supporting Variants
SamplesHG03941
Known GenesCBWD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13373813
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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