A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638421



Internal ID21830468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41757543..41786721hg38UCSC Ensembl
chr21:43177703..43206881hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3829179
hg1929179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047673
Supporting Variants
Samples
Known GenesRIPK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638421
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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