A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669176



Internal ID21617481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61397380..61397380hg38UCSC Ensembl
chr20:59972436..59972436hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386074
hg196074
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117564
SamplesHG02011
Known GenesCDH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669176
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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