A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023021



Internal ID83054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61519000..61654000hg38UCSC Ensembl
chr9:44726838..44861838hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38135001
hg19135001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487172
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023021
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008202


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