A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946433



Internal ID21366504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46229146..46229146hg38UCSC Ensembl
chr21:47649060..47649060hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187367
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946433
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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