A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545571



Internal ID21869926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48979068..49067308hg38UCSC Ensembl
chr4:48981085..49069325hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3888241
hg1988241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997347
Supporting Variants
Samples
Known GenesCWH43
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545571
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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