A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974159



Internal ID22749094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69993373..69993373hg38UCSC Ensembl
chr15:70285712..70285712hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974159
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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