A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948467



Internal ID33017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20003882..20017119hg38UCSC Ensembl
chr4:20005505..20018742hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3813238
hg1913238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948467
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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