A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097149



Internal ID20664189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17016901..17046500hg38UCSC Ensembl
chr3:17058393..17087992hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3829600
hg1929600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367513
Supporting Variants
Samples
Known GenesPLCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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