A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205208



Internal ID20772248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8881266..8971053hg38UCSC Ensembl
chr1:8941325..9031112hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3889788
hg1989788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320847
Supporting Variants
Samples
Known GenesCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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