A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641292



Internal ID21833339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29018677..29018990hg38UCSC Ensembl
chr21:30390998..30391311hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057040
Supporting Variants
Samples
Known GenesRWDD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641292
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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