A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104980



Internal ID21493858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38124422..38124422hg38UCSC Ensembl
chr19:38615062..38615062hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664087
Supporting Variants
SamplesNA19238
Known GenesSIPA1L3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104980
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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