A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071716



Internal ID20638756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26558628..26559225hg38UCSC Ensembl
chr21:27930947..27931544hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542454
Supporting Variants
Samples
Known GenesCYYR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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