A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439116



Internal ID22105293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70408984..70408984hg38UCSC Ensembl
chr9:73023900..73023900hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765491
Samples
Known GenesKLF9
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439116
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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