A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439614



Internal ID22105791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24683759..24683759hg38UCSC Ensembl
chr6:24683987..24683987hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763248
Samples
Known GenesACOT13
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439614
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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