A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489392



Internal ID21146945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63501416..63506346hg38UCSC Ensembl
chr14:63968134..63973064hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg384931
hg194931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020677
Samples
Known GenesPPP2R5E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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