A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501823



Internal ID20875060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94143067..94173350hg38UCSC Ensembl
chr14:94609404..94639687hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3830284
hg1930284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501823
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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