A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133153



Internal ID21456676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26631671..26631908hg38UCSC Ensembl
chr3:26673162..26673399hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580826
Supporting Variants
SamplesHG02587
Known GenesLRRC3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133153
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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