A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952581



Internal ID35745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83082075..83082110hg38UCSC Ensembl
chr4:84003228..84003263hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952581
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003278


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