A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399965



Internal ID22457835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42859696..42859696hg38UCSC Ensembl
chr22:43255702..43255702hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399965
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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