A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445927



Internal ID22112105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63853700..63853700hg38UCSC Ensembl
chr20:62485053..62485053hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764844
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445927
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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