A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069480



Internal ID20636520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18053101..18054800hg38UCSC Ensembl
chr21:19425419..19427118hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539023
Supporting Variants
Samples
Known GenesCHODL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069480
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