A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15768458



Internal ID22102932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120328596..120328596hg38UCSC Ensembl
chr11:120199305..120199305hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4448107
Supporting Variants
Samples
Known GenesTMEM136
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15768458
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer