A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449282



Internal ID22115459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168867268..168867268hg38UCSC Ensembl
chr2:169723778..169723778hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3816944
hg1916944
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762743
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449282
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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