A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467736



Internal ID245547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47965632..47966546hg38UCSC Ensembl
chr4:47967649..47968563hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16950000
Samples
Known GenesCNGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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