A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445786



Internal ID22503656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131742356..131746874hg38UCSC Ensembl
chr9:134617743..134622261hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384519
hg194519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445786
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.042


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