A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012092



Internal ID20579132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66992653..66993310hg38UCSC Ensembl
chr13:67566785..67567442hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480173
Supporting Variants
Samples
Known GenesPCDH9, PCDH9-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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