A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668096



Internal ID21616402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61059908..61059908hg38UCSC Ensembl
chr20:59634964..59634964hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381008
hg191008
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117193
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668096
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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