A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437649



Internal ID22495519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34546673..34546797hg38UCSC Ensembl
chr9:34546671..34546795hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437649
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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