A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497046



Internal ID274105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67201600..67211903hg38UCSC Ensembl
chr13:67775732..67786035hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3810304
hg1910304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691657
Samples
Known GenesPCDH9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497046
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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