A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133776



Internal ID21476553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140549411..140550865hg38UCSC Ensembl
chr3:140268253..140269707hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381455
hg191455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565781
Supporting Variants
SamplesHG03486
Known GenesCLSTN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133776
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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