A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194445



Internal ID21333343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68866111..68866111hg38UCSC Ensembl
chr14:69332828..69332828hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3930939
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194445
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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