A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476750



Internal ID21134303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64667149..64687561hg38UCSC Ensembl
chr14:65133867..65154279hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3820413
hg1920413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476750
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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