A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253278



Internal ID20820318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52115025..52115553hg38UCSC Ensembl
chr20:50731564..50732092hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597277
Supporting Variants
Samples
Known GenesZFP64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253278
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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