A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938975



Internal ID21359044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39033513..39033513hg38UCSC Ensembl
chr14:39502717..39502717hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195090
SamplesHG002
Known GenesSEC23A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938975
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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