A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226278



Internal ID20793318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80606461..80636041hg38UCSC Ensembl
chr9:83221376..83250956hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3829581
hg1929581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226278
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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