A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121081



Internal ID21499967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13514617..13514700hg38UCSC Ensembl
chr3:13556117..13556200hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582968
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121081
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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