A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185414



Internal ID20752455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76225228..76230282hg38UCSC Ensembl
chr9:78840144..78845198hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385055
hg195055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436133
Supporting Variants
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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