A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943918



Internal ID21363987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188636933..188636933hg38UCSC Ensembl
chr3:188354721..188354721hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191017
SamplesHG002
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943918
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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