A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18011616



Internal ID20578656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66356564..66356953hg38UCSC Ensembl
chr13:66930696..66931085hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477746
Supporting Variants
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18011616
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00192


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