A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512083



Internal ID20885413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99103453..99104698hg38UCSC Ensembl
chr14:99569790..99571035hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512083
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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