A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059962



Internal ID21453649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11239516..11239516hg38UCSC Ensembl
chr1:11299573..11299573hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606922
Supporting Variants
SamplesHG02011
Known GenesMTOR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059962
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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