A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489667



Internal ID21147220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55801521..55805592hg38UCSC Ensembl
chr14:56268239..56272310hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg384072
hg194072
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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