A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551299



Internal ID21875654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47965627..47966546hg38UCSC Ensembl
chr4:47967644..47968563hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997522
Supporting Variants
Samples
Known GenesCNGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551299
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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