A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519023



Internal ID295382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73565734..73566473hg38UCSC Ensembl
chr17:71561873..71562612hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714502
Samples
Known GenesSDK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519023
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