A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644417



Internal ID21836464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43743503..43743503hg38UCSC Ensembl
chr21:45163384..45163384hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110689
Supporting Variants
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644417
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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