A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937666



Internal ID21357735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105015398..105015398hg38UCSC Ensembl
chr14:105481735..105481735hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195198
SamplesHG002
Known GenesCDCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937666
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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