A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913696



Internal ID22688912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117644189..117646003hg38UCSC Ensembl
chr9:120406467..120408281hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg381815
hg191815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913696
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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