A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440921



Internal ID22107099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89872382..89872382hg38UCSC Ensembl
chr6:90582101..90582101hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382338
hg192338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765445
Samples
Known GenesCASP8AP2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440921
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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