A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194988



Internal ID21333890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55303275..55303275hg38UCSC Ensembl
chr15:55595473..55595473hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948783
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194988
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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