A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438169



Internal ID22496039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121326448..121326536hg38UCSC Ensembl
chr9:124088726..124088814hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914545
Supporting Variants
Samples
Known GenesGSN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438169
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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