A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523825



Internal ID300044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68829786..68832538hg38UCSC Ensembl
chr16:68863689..68866441hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382753
hg192753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708516
Samples
Known GenesCDH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523825
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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