A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602079



Internal ID21794126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40566268..40568275hg38UCSC Ensembl
chr15:40858467..40860474hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382008
hg192008
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602079
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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