A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430274



Internal ID22488144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109523565..109524281hg38UCSC Ensembl
chr9:112285845..112286561hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430274
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.04


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