A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554282



Internal ID20927385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45833389..45834008hg38UCSC Ensembl
chr21:47253303..47253922hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072840
Samples
Known GenesLOC100129027
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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