A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400182



Internal ID22458052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49720929..49720929hg38UCSC Ensembl
chr22:50114577..50114577hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400182
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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