A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128076



Internal ID21412066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169167961..169167961hg38UCSC Ensembl
chr3:168885749..168885749hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607562
Supporting Variants
SamplesHG00513
Known GenesMECOM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128076
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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