A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448547



Internal ID22114724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133932259..133932259hg38UCSC Ensembl
chr11:133802154..133802154hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759902
Samples
Known GenesIGSF9B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448547
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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