A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069594



Internal ID20636634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:20295710..20844915hg38UCSC Ensembl
chr21:21668022..22217233hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38549206
hg19549212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537787
Supporting Variants
Samples
Known GenesLINC00320
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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