A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923958



Internal ID22699185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132541472..132541661hg38UCSC Ensembl
chr9:135416859..135417048hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431664
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923958
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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