A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548829



Internal ID20922007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10159101..10163500hg38UCSC Ensembl
chr21:10637129..10641528hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548829
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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