A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553426



Internal ID21877781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:63543046..63554869hg38UCSC Ensembl
chr4:64408764..64420587hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3811824
hg1911824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998286
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553426
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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