A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193706



Internal ID21332599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101358101..101358101hg38UCSC Ensembl
chr14:101824438..101824438hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941960
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193706
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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