A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937189



Internal ID21357259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59427635..59427635hg38UCSC Ensembl
chr14:59894353..59894353hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194852
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937189
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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