A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403021



Internal ID22460891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31495982..31495982hg38UCSC Ensembl
chr22:31891968..31891968hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403021
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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