A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232963



Internal ID20800003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34331058..34409105hg38UCSC Ensembl
chr9:34331056..34409103hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3878048
hg1978048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451770
Supporting Variants
Samples
Known GenesC9orf24, FAM219A, KIAA1161, NUDT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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