A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668225



Internal ID21616530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19723625..19723625hg38UCSC Ensembl
chr20:19704269..19704269hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116068
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668225
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer