A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195192



Internal ID21334098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104683310..104683310hg38UCSC Ensembl
chr14:105149647..105149647hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940947
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195192
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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