A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705457



Internal ID21377733
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 StatusS
Merged Variantsnsv4390439
Supporting Variants
Samples
Known GenesTDG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705457
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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