A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386711



Internal ID22444581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73724911..73724911hg38UCSC Ensembl
chr15:74017252..74017252hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386711
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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