A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947892



Internal ID32624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32552322..32552422hg38UCSC Ensembl
chr4:32553944..32554044hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438652
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947892
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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