A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259195



Internal ID20826235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111805263..111806622hg38UCSC Ensembl
chr3:111524110..111525469hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg381360
hg191360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564900
Supporting Variants
Samples
Known GenesPHLDB2, PLCXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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