A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747797



Internal ID20523818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38913904..38914732hg38UCSC Ensembl
chr21:40285828..40286656hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747797
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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