A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436862



Internal ID22494732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119168600..119168658hg38UCSC Ensembl
chr9:121930878..121930936hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918966
Supporting Variants
Samples
Known GenesBRINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436862
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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