A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16912329



Internal ID8970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33225909..33229905hg38UCSC Ensembl
chr2:33450976..33454972hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg383997
hg193997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452014
Supporting Variants
Samples
Known GenesLTBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16912329
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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