A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012062



Internal ID20579102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66781467..66872048hg38UCSC Ensembl
chr13:67355599..67446180hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3890582
hg1990582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489218
Supporting Variants
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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