A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268636



Internal ID20835676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146769180..146770107hg38UCSC Ensembl
chr5:146148743..146149670hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575166
Supporting Variants
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268636
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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