A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409716



Internal ID22467586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186376962..186379013hg38UCSC Ensembl
chr3:186094751..186096802hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382052
hg192052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409716
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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