A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443666



Internal ID22109847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39326085..39326085hg38UCSC Ensembl
chr20:37954728..37954728hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757880
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443666
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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