A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023053



Internal ID83078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62397369..62507450hg38UCSC Ensembl
chr9:46708670..46818751hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38110082
hg19110082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142197
Supporting Variants
Samples
Known GenesKGFLP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023053
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0381


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