A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133356



Internal ID21500137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193436806..193437117hg38UCSC Ensembl
chr3:193154595..193154906hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566490
Supporting Variants
SamplesNA19239
Known GenesATP13A4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133356
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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