A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446094



Internal ID22112273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16225124..16225124hg38UCSC Ensembl
chr2:16406392..16406392hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757492
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446094
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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