A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128696



Internal ID21468673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36891723..36891723hg38UCSC Ensembl
chr22:37287765..37287765hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665158
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128696
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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