A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737984



Internal ID20513949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111296652..111296740hg38UCSC Ensembl
chr12:111734456..111734544hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273110
Samples
Known GenesCUX2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737984
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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