A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948799



Internal ID33226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35948553..35948604hg38UCSC Ensembl
chr4:35950175..35950226hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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