A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395335



Internal ID22453205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30478308..30478308hg38UCSC Ensembl
chr22:30874295..30874295hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395335
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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