A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259353



Internal ID20826393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218613079..218614091hg38UCSC Ensembl
chr2:219477802..219478814hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381013
hg191013
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551496
Supporting Variants
Samples
Known GenesPLCD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259353
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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