A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025867



Internal ID84982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96356588..96356683hg38UCSC Ensembl
chr9:99118870..99118965hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486668
Supporting Variants
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025867
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02123


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