A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537893



Internal ID20911222
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 StatusM
Merged Variants
Supporting Variantsnssv18071570
Samples
Known GenesZBTB21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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