A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193806



Internal ID21332698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79503530..79503530hg38UCSC Ensembl
chr15:79795872..79795872hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926991
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193806
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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