A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443907



Internal ID22110088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38653032..38653032hg38UCSC Ensembl
chr20:37281675..37281675hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761887
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443907
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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