A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949966



Internal ID21370035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33156871..33156871hg38UCSC Ensembl
chr21:34529177..34529177hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15188297
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949966
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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