A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954103



Internal ID36730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118828688..118828739hg38UCSC Ensembl
chr4:119749843..119749894hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412654
Supporting Variants
Samples
Known GenesSEC24D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954103
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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