A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232170



Internal ID20799210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32217204..32230267hg38UCSC Ensembl
chr9:32217202..32230265hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3813064
hg1913064
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426315
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232170
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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