A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074978



Internal ID20642018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46315237..46323758hg38UCSC Ensembl
chr22:46711134..46719655hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg388522
hg198522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546261
Supporting Variants
Samples
Known GenesGTSE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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