A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446785



Internal ID22112962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101041051..101041051hg38UCSC Ensembl
chr11:100911782..100911782hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766667
Samples
Known GenesPGR
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446785
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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