A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098331



Internal ID21450451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94529371..94529371hg38UCSC Ensembl
chr12:94923147..94923147hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656233
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098331
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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