A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484071



Internal ID21141624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64726123..64729350hg38UCSC Ensembl
chr14:65192841..65196068hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg383228
hg193228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020703
Samples
Known GenesPLEKHG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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