A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389277



Internal ID21380412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18214147..18214660hg38UCSC Ensembl
chr10:18503076..18503589hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704810
Samples
Known GenesCACNB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389277
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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