A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218754



Internal ID20785794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53860643..53862034hg38UCSC Ensembl
chr10:55620403..55621794hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590941
Supporting Variants
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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