A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935969



Internal ID21356038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150245146..150245146hg38UCSC Ensembl
chr3:149962933..149962933hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189892
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935969
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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