A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914798



Internal ID10611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:56431226..56471360hg38UCSC Ensembl
chr2:56658361..56698495hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3840135
hg1940135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914798
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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