A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101379



Internal ID21428900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63198864..63198864hg38UCSC Ensembl
chr18:60866097..60866097hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662555
Supporting Variants
SamplesHG00731
Known GenesBCL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101379
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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