A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022224



Internal ID21931567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66650969..66744685hg38UCSC Ensembl
chr13:67225101..67318817hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3893717
hg1993717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601788
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022224
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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