A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443598



Internal ID22109781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125426489..125426614hg38UCSC Ensembl
chr11:125296385..125296510hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768228
Samples
Known GenesPKNOX2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443598
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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