A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551559



Internal ID21875914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83017083..83017165hg38UCSC Ensembl
chr4:83938236..83938318hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551559
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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