A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438648



Internal ID22104828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890253..45890253hg38UCSC Ensembl
chr3:45931745..45931745hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766684
Samples
Known GenesCCR9, LZTFL1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438648
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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