A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486668



Internal ID264027
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 StatusM
Merged Variants
Supporting Variantsnssv17025867
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486668
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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