A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442116



Internal ID22108299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116599211..116599211hg38UCSC Ensembl
chr12:117037016..117037016hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758841
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442116
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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