A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424849



Internal ID22482719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17066673..17067038hg38UCSC Ensembl
chr3:17108165..17108530hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903080
Supporting Variants
Samples
Known GenesPLCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424849
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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