A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389701



Internal ID21380836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18268817..18268870hg38UCSC Ensembl
chr11:18290364..18290417hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705047
Samples
Known GenesSAA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389701
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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