A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228388



Internal ID20795428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121500987..121510887hg38UCSC Ensembl
chr8:122513227..122523127hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg389901
hg199901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432731
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228388
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00025


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