A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398495



Internal ID22456365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37946222..37948609hg38UCSC Ensembl
chr22:38342229..38344616hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382388
hg192388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965645
Supporting Variants
Samples
Known GenesC22orf23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398495
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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