A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929985



Internal ID20726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4993555..4993585hg38UCSC Ensembl
chr3:5035240..5035270hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929985
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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