A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491225



Internal ID21148778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69601395..69609143hg38UCSC Ensembl
chr14:70068112..70075860hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg387749
hg197749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491225
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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