A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512351



Internal ID20885684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104319106..104473632hg38UCSC Ensembl
chr14:104785443..104939969hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38154527
hg19154527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512351
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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