A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401119



Internal ID22458989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21749869..21750891hg38UCSC Ensembl
chr22:22104158..22105180hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401119
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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