A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445503



Internal ID22111682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74987611..74987611hg38UCSC Ensembl
chr13:75561748..75561748hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761909
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445503
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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