A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477429



Internal ID21134982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28994847..29003751hg38UCSC Ensembl
chr14:29464053..29472957hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg388905
hg198905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477429
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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