A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490132



Internal ID21147685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66663946..66825803hg38UCSC Ensembl
chr13:67238078..67399935hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38161858
hg19161858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1892n223
Supporting Variantsnssv18011831
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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