A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488593



Internal ID21146146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54823336..54835750hg38UCSC Ensembl
chr14:55290054..55302468hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3812415
hg1912415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488593
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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