A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667162



Internal ID21615469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63101730..63101730hg38UCSC Ensembl
chr20:61733082..61733082hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384389
hg194389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117629
SamplesNA12329
Known GenesHAR1A, HAR1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667162
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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