A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947011



Internal ID32033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24879249..24879370hg38UCSC Ensembl
chr4:24880871..24880992hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440420
Supporting Variants
Samples
Known GenesCCDC149
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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