A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926438



Internal ID21346507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10129134..10129134hg38UCSC Ensembl
chr21:10607162..10607162hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186432
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926438
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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