A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071488



Internal ID20638528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41294474..41294872hg38UCSC Ensembl
chr21:42666401..42666799hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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