A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432816



Internal ID22490686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69832620..69832620hg38UCSC Ensembl
chr9:72447536..72447536hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959994
Supporting Variants
Samples
Known GenesC9orf135
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432816
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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