A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390818



Internal ID21381953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100126315..100131112hg38UCSC Ensembl
chr13:100778569..100783366hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384798
hg194798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705667
Samples
Known GenesPCCA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390818
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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