A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385408



Internal ID22443278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45346265..45346265hg38UCSC Ensembl
chr15:45638463..45638463hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385408
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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