A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445824



Internal ID22112001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45101590..45101590hg38UCSC Ensembl
chr11:45123141..45123141hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760796
Samples
Known GenesPRDM11
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445824
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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