A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952837



Internal ID35910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96648408..96664784hg38UCSC Ensembl
chr4:97569559..97585935hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3816377
hg1916377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455425
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952837
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