A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621168



Internal ID21569473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140087085..140087085hg38UCSC Ensembl
chr3:139805927..139805927hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129227
SamplesHG00732
Known GenesCLSTN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621168
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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