A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663402



Internal ID21611707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113813640..113813640hg38UCSC Ensembl
chr12:114251445..114251445hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077800
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663402
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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