A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404195



Internal ID183551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82901653..82901704hg38UCSC Ensembl
chr4:83822806..83822857hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951479
Samples
Known GenesTHAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404195
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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