A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626177



Internal ID21818224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23876224..23885897hg38UCSC Ensembl
chr20:23856861..23866534hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg389674
hg199674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045183
Supporting Variants
Samples
Known GenesCST5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626177
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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