A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074456



Internal ID20641496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44674945..44675250hg38UCSC Ensembl
chr22:45070825..45071130hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542780
Supporting Variants
Samples
Known GenesPRR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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