A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934284



Internal ID22709607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43768680..43768730hg38UCSC Ensembl
chr17:41846048..41846098hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386107
Samples
Known GenesDUSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934284
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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