A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957949



Internal ID39280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138087201..138088984hg38UCSC Ensembl
chr4:139008355..139010138hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463042
Supporting Variants
Samples
Known GenesLINC00616
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957949
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