A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533607



Internal ID309495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76268596..76274419hg38UCSC Ensembl
chr17:74264677..74270500hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg385824
hg195824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714702
Samples
Known GenesQRICH2, UBALD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533607
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