A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235814



Internal ID20802854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20347685..20349068hg38UCSC Ensembl
chr14:20815844..20817227hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585331
Supporting Variants
Samples
Known GenesPARP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235814
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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