A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497432



Internal ID20870638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105136201..105186300hg38UCSC Ensembl
chr14:105602538..105652637hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3850100
hg1950100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184012
Samples
Known GenesJAG2, MIR6765, NUDT14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497432
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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