A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290755



Internal ID20499973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61273466..61273466hg38UCSC Ensembl
chr20:59848522..59848522hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764350
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290755
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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