A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440897



Internal ID22107075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43415778..43415778hg38UCSC Ensembl
chr13:43989914..43989914hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760966
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440897
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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