A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190200



Internal ID20757240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64549501..64554100hg38UCSC Ensembl
chr14:65016219..65020818hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495568
Supporting Variants
Samples
Known GenesPPP1R36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00361


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