A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236804



Internal ID20803844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141469101..141632000hg38UCSC Ensembl
chr8:142479201..142642100hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38162900
hg19162900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419226
Supporting Variants
Samples
Known GenesMROH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236804
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00499


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