A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944190



Internal ID21364259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32200011..32200011hg38UCSC Ensembl
chr14:32669217..32669217hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194810
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944190
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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