A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997522



Internal ID21906865
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 StatusM
Merged Variants
Supporting Variantsnssv17551299
Samples
Known GenesCNGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997522
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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