A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222283



Internal ID20789323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34250156..34444322hg38UCSC Ensembl
chr9:34250154..34444320hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38194167
hg19194167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440375
Supporting Variants
Samples
Known GenesC9orf24, FAM219A, KIAA1161, KIF24, NUDT2, UBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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