A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627225



Internal ID21819272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61793845..61793845hg38UCSC Ensembl
chr20:60368901..60368901hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105230
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627225
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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