A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390022



Internal ID21381157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111514469..111514741hg38UCSC Ensembl
chr11:111385194..111385466hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705228
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390022
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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