A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933273



Internal ID21353342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15737522..15737522hg38UCSC Ensembl
chr3:15779029..15779029hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189671
SamplesHG002
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933273
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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