A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027965



Internal ID21937308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66845072..67848802hg38UCSC Ensembl
chr13:67419204..68422934hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg381003731
hg191003731
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600267
Samples
Known GenesPCDH9, PCDH9-AS2, PCDH9-AS3, PCDH9-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027965
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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