A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080061



Internal ID21483506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38317557..38317557hg38UCSC Ensembl
chr12:38711359..38711359hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663886
Supporting Variants
SamplesHG03732
Known GenesALG10B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080061
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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