A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766311



Internal ID22100783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1766441..1766441hg38UCSC Ensembl
chr19:1766440..1766440hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4441255
Supporting Variants
Samples
Known GenesONECUT3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766311
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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