A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448099



Internal ID22114277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127720799..127720799hg38UCSC Ensembl
chr9:130483078..130483078hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762936
Samples
Known GenesTTC16
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448099
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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