A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613682



Internal ID21561987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171601495..171601495hg38UCSC Ensembl
chr3:171319285..171319285hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124574
SamplesNA19239
Known GenesPLD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613682
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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