A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955603



Internal ID37709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109466800..109470252hg38UCSC Ensembl
chr4:110387956..110391408hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383453
hg193453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459901
Supporting Variants
Samples
Known GenesSEC24B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955603
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