A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491607



Internal ID268840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:625337..722197hg38UCSC Ensembl
chr9:625337..722197hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3896861
hg1996861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv518n206
Supporting Variantsnssv17019578
Samples
Known GenesKANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491607
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