A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083801



Internal ID21510973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65965601..65965601hg38UCSC Ensembl
chr15:66257939..66257939hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663034
Supporting Variants
SamplesNA24385
Known GenesMEGF11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083801
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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