A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909849



Internal ID7334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15583043..15583739hg38UCSC Ensembl
chr2:15723167..15723863hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909849
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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