A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665849



Internal ID21614155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61273526..61273526hg38UCSC Ensembl
chr20:59848582..59848582hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117225
SamplesHG00731
Known GenesCDH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665849
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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