A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884689



Internal ID22659672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60052452..60063540hg38UCSC Ensembl
chr20:58627507..58638595hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811089
hg1911089
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486747
Samples
Known GenesC20orf197
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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