A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446542



Internal ID22112721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84099802..84099802hg38UCSC Ensembl
chr11:83810845..83810845hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761226
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446542
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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