A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135364



Internal ID21502884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70009580..70018522hg38UCSC Ensembl
chr3:70058731..70067673hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388943
hg198943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566822
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135364
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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