A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221284



Internal ID20788324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69001431..69015947hg38UCSC Ensembl
chr8:69913666..69928182hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3814517
hg1914517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434391
Supporting Variants
Samples
Known GenesLOC100505718
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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