A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077824



Internal ID21509844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114874417..114874417hg38UCSC Ensembl
chr12:115312222..115312222hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663452
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077824
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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