A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610468



Internal ID21558773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188180797..188180797hg38UCSC Ensembl
chr3:187898585..187898585hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120446
SamplesHG00732
Known GenesFLJ42393, LPP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610468
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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