A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074692



Internal ID20641732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48179387..48179737hg38UCSC Ensembl
chr22:48575199..48575549hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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