A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706534



Internal ID21378810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36807994..36808127hg38UCSC Ensembl
chr20:35436397..35436530hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392538
Supporting Variants
Samples
Known GenesSOGA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706534
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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