A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932798



Internal ID21352867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56731592..56731592hg38UCSC Ensembl
chr3:56765620..56765620hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189766
SamplesHG002
Known GenesARHGEF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932798
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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