A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074702



Internal ID21489779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45101631..45101631hg38UCSC Ensembl
chr11:45123182..45123182hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653195
Supporting Variants
SamplesNA19238
Known GenesPRDM11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074702
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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