A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132938



Internal ID21452364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169534232..169534232hg38UCSC Ensembl
chr3:169252020..169252020hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614387
Supporting Variants
SamplesHG01596
Known GenesMECOM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132938
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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