A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101377



Internal ID21493309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63169264..63169328hg38UCSC Ensembl
chr18:60836497..60836561hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596225
Supporting Variants
SamplesNA19238
Known GenesBCL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101377
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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