A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446140



Internal ID22112319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58404364..58404364hg38UCSC Ensembl
chr11:58171837..58171837hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767880
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446140
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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