A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483057



Internal ID21140610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26664661..26932283hg38UCSC Ensembl
chr14:27133867..27401489hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38267623
hg19267623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182135
Samples
Known GenesMIR4307
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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