A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445263



Internal ID22111443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58822745..58822745hg38UCSC Ensembl
chr13:59396879..59396879hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757639
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445263
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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