A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390439



Internal ID21381574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103961559..103967839hg38UCSC Ensembl
chr12:104355337..104361617hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg386281
hg196281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705457
Samples
Known GenesTDG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390439
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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