A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480758



Internal ID21138311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49853709..49862689hg38UCSC Ensembl
chr14:50320427..50329407hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg388981
hg198981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480758
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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