A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224958



Internal ID20791998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140940775..140965675hg38UCSC Ensembl
chr8:141950874..141975774hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3824901
hg1924901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434267
Supporting Variants
Samples
Known GenesPTK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224958
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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