A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135102



Internal ID21505971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38783336..38783336hg38UCSC Ensembl
chr22:39179341..39179341hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667377
Supporting Variants
SamplesNA19983
Known GenesDNAL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135102
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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