A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441283



Internal ID22107463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45111212..45111405hg38UCSC Ensembl
chr11:45132763..45132956hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758339
Samples
Known GenesPRDM11
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441283
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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