A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477187



Internal ID21134740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50181215..50197377hg38UCSC Ensembl
chr14:50647933..50664095hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3816163
hg1916163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193972
Samples
Known GenesSOS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477187
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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