A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916201



Internal ID22691420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35228468..35228567hg38UCSC Ensembl
chr9:35228465..35228564hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439462
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916201
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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