A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236584



Internal ID20803624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25428801..25517400hg38UCSC Ensembl
chr9:25428799..25517398hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3888600
hg1988600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434380
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236584
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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