A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074501



Internal ID20641541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41364054..41374401hg38UCSC Ensembl
chr22:41760058..41770405hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3810348
hg1910348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537592
Supporting Variants
Samples
Known GenesTEF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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