A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490216



Internal ID21147769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77081868..77096803hg38UCSC Ensembl
chr14:77548211..77563146hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3814936
hg1914936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490216
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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