A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132991



Internal ID21415903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38963395..38963450hg38UCSC Ensembl
chr3:39004886..39004941hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569354
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132991
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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