A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624086



Internal ID21572391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195337898..195337898hg38UCSC Ensembl
chr3:195058627..195058627hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136402
SamplesHG02492
Known GenesACAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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