A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444091



Internal ID22110272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50258483..50258483hg38UCSC Ensembl
chr20:48875020..48875020hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757506
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444091
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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