A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077084



Internal ID21473694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106302405..106302405hg38UCSC Ensembl
chr12:106696183..106696183hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646529
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077084
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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