A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031111



Internal ID88443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134195000..134251536hg38UCSC Ensembl
chr9:137091194..137143382hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3856537
hg1952189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031111
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000627


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