A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389610



Internal ID21380745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27259431..27259539hg38UCSC Ensembl
chr2:27482299..27482407hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705826
Samples
Known GenesSLC30A3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389610
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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