A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15756913



Internal ID22091389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86298263..86298263hg38UCSC Ensembl
chr15:86841494..86841494hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447075
Supporting Variants
Samples
Known GenesAGBL1, AGBL1-AS1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15756913
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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