A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492466



Internal ID21150019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81242901..81249000hg38UCSC Ensembl
chr14:81709245..81715344hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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