A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099357



Internal ID21410016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67989945..67989945hg38UCSC Ensembl
chr12:68383725..68383725hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg386619
hg196619
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650722
Supporting Variants
SamplesHG00512
Known GenesIFNG-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099357
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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