A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484639



Internal ID21142192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38254501..38256500hg38UCSC Ensembl
chr14:38723706..38725705hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196854
Samples
Known GenesCLEC14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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