A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123908



Internal ID21451019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176477012..176480163hg38UCSC Ensembl
chr3:176194800..176197951hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383152
hg193152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565966
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123908
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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