A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016804



Internal ID20583844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24224024..24228609hg38UCSC Ensembl
chr14:24693230..24697815hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384586
hg194586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481133
Supporting Variants
Samples
Known GenesNEDD8, NEDD8-MDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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