A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914875



Internal ID10669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60846728..60855409hg38UCSC Ensembl
chr2:61073863..61082544hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg388682
hg198682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451731
Supporting Variants
Samples
Known GenesFLJ16341
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914875
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer