A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077109



Internal ID21444335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107809481..107809481hg38UCSC Ensembl
chr12:108203258..108203258hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662568
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077109
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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