A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608832



Internal ID21557137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:93885860..93885860hg38UCSC Ensembl
chr3:93604704..93604704hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132301
SamplesHG03371
Known GenesPROS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608832
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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