A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483150



Internal ID21140703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66689272..66714904hg38UCSC Ensembl
chr14:67155990..67181622hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3825633
hg1925633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182332
Samples
Known GenesGPHN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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