A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465006



Internal ID242877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149368586..149369137hg38UCSC Ensembl
chr4:150289738..150290289hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465006
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