A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948641



Internal ID33130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28532808..28532845hg38UCSC Ensembl
chr4:28534430..28534467hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948641
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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