A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637166



Internal ID21829213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32281256..32282805hg38UCSC Ensembl
chr20:30869059..30870608hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049601
Supporting Variants
Samples
Known GenesKIF3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637166
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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