A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487168



Internal ID21144721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59454401..59496600hg38UCSC Ensembl
chr14:59921119..59963318hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3842200
hg1942200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191215
Samples
Known GenesGPR135, JKAMP, L3HYPDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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