A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025871



Internal ID84984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96410089..96411834hg38UCSC Ensembl
chr9:99172371..99174116hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381746
hg191746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485896
Supporting Variants
Samples
Known GenesZNF367
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer