A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092102



Internal ID20659142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111785800..111786582hg38UCSC Ensembl
chr3:111504647..111505429hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367791
Supporting Variants
Samples
Known GenesPHLDB2, PLCXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092102
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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