A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900897



Internal ID1396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2623479..2624989hg38UCSC Ensembl
chr2:2627251..2628761hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900897
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002966


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