A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445266



Internal ID22111446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60255312..60255312hg38UCSC Ensembl
chr13:60829446..60829446hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759805
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445266
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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