A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618695



Internal ID21810742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36801430..36801430hg38UCSC Ensembl
chr20:35429833..35429833hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38852
hg19852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112320
Supporting Variants
Samples
Known GenesSOGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618695
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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