A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909954



Internal ID7412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9950888..9950940hg38UCSC Ensembl
chr2:10091017..10091069hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909954
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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