A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522681



Internal ID298943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33126858..33127168hg38UCSC Ensembl
chr17:31453876..31454186hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712691
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522681
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