A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490124



Internal ID21147677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21272974..21279207hg38UCSC Ensembl
chr14:21741133..21747366hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg386234
hg196234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490124
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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