A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222119



Internal ID20789159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120063150..120081413hg38UCSC Ensembl
chr8:121075389..121093652hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3818264
hg1918264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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