A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217626



Internal ID20784666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49035201..49045500hg38UCSC Ensembl
chr8:49947760..49958059hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217626
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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