A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444293



Internal ID22110473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24212397..24212397hg38UCSC Ensembl
chr14:24681603..24681603hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765506
Samples
Known GenesCHMP4A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444293
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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