A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598020



Internal ID21790064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66621684..66624816hg38UCSC Ensembl
chr13:67195816..67198948hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg383133
hg193133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022301
Supporting Variants
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598020
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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