A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654524



Internal ID21602829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45101590..45101590hg38UCSC Ensembl
chr11:45123141..45123141hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074700
SamplesNA19239
Known GenesPRDM11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654524
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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