A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470299



Internal ID21127852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106121274..106122523hg38UCSC Ensembl
chr12:106515052..106516301hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996102
Samples
Known GenesNUAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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