A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443746



Internal ID22109927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108247494..108247494hg38UCSC Ensembl
chr9:111009774..111009774hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760269
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443746
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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