A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941282



Internal ID22716704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78577753..78601592hg38UCSC Ensembl
chr17:76573835..76597674hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3823840
hg1923840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941282
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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