A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229993



Internal ID20797033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22882401..23152700hg38UCSC Ensembl
chr9:22882400..23152699hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38270300
hg19270300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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