A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503686



Internal ID20876942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95534101..95536400hg38UCSC Ensembl
chr14:96000438..96002737hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191705
Samples
Known GenesGLRX5, SNHG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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