A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661829



Internal ID21610134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:34199306..34199306hg38UCSC Ensembl
chr12:34352241..34352241hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086301
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661829
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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