A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447437



Internal ID22113614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31226463..31226463hg38UCSC Ensembl
chr22:31622449..31622449hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757794
Samples
Known GenesLIMK2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447437
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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