A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967268



Internal ID22742203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69835681..69835681hg38UCSC Ensembl
chr9:72450597..72450597hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448524
Samples
Known GenesC9orf135
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967268
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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