A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071570



Internal ID20638610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41986532..41987136hg38UCSC Ensembl
chr21:43406641..43407245hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537893
Supporting Variants
Samples
Known GenesZBTB21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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