A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493500



Internal ID21151053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23809487..23854867hg38UCSC Ensembl
chr14:24278696..24324076hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3845381
hg1945381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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