A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939551



Internal ID21359620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101419640..101419640hg38UCSC Ensembl
chr14:101885977..101885977hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193707
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939551
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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