A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503713



Internal ID20876969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95155501..95158500hg38UCSC Ensembl
chr14:95621838..95624837hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177528
Samples
Known GenesDICER1, DICER1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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