A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548788



Internal ID20921970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31989565..32018244hg38UCSC Ensembl
chr21:33361878..33390557hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3828680
hg1928680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206647
Samples
Known GenesHUNK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548788
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