A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227095



Internal ID20794135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53891940..53892056hg38UCSC Ensembl
chr10:55651700..55651816hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593386
Supporting Variants
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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