A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980896



Internal ID20547936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54067468..54069582hg38UCSC Ensembl
chr10:55827228..55829342hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445063
Supporting Variants
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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