A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386203



Internal ID22444073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70581051..70581128hg38UCSC Ensembl
chr15:70873390..70873467hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386203
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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