A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437623



Internal ID22495493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92860371..92860454hg38UCSC Ensembl
chr9:95622653..95622736hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921580
Supporting Variants
Samples
Known GenesZNF484
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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