A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595966



Internal ID21544573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43176582..43178121hg38UCSC Ensembl
chr15:43468780..43470319hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381540
hg191540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087798
SamplesHG03065
Known GenesTMEM62
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595966
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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