A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022523



Internal ID82696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40691948..40886100hg38UCSC Ensembl
chr9:66664196..66839128hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38194153
hg19174933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022523
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.04782


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