A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446432



Internal ID22112611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35864267..35864585hg38UCSC Ensembl
chr13:36438404..36438722hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764918
Samples
Known GenesDCLK1, MIR548F5
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446432
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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