A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096341



Internal ID21492525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76120698..76120698hg38UCSC Ensembl
chr12:76514478..76514478hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660807
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096341
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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