A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487911



Internal ID21145464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62086101..62089400hg38UCSC Ensembl
chr14:62552819..62556118hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191310
Samples
Known GenesSYT16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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