A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915067



Internal ID10789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68301708..68305612hg38UCSC Ensembl
chr2:68528840..68532744hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383905
hg193905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441485
Supporting Variants
Samples
Known GenesCNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915067
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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