A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367791



Internal ID21025344
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 StatusM
Merged Variants
Supporting Variantsnssv18092102
Samples
Known GenesPHLDB2, PLCXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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