A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445954



Internal ID22112132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64178465..64178465hg38UCSC Ensembl
chr20:62809818..62809818hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761118
Samples
Known GenesMYT1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445954
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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