A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907799



Internal ID5982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8105962..8146962hg38UCSC Ensembl
chr1:8166022..8207022hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3841001
hg1941001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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