A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953421



Internal ID36301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102304620..102304748hg38UCSC Ensembl
chr4:103225777..103225905hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454692
Supporting Variants
Samples
Known GenesSLC39A8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953421
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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