A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077645



Internal ID21466678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122072860..122072860hg38UCSC Ensembl
chr12:122510766..122510766hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651958
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077645
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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