A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911622



Internal ID22686837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36253766..36254254hg38UCSC Ensembl
chr9:36253763..36254251hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447400
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911622
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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