A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444852



Internal ID22111032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49886587..49886587hg38UCSC Ensembl
chr13:50460723..50460723hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381665
hg191665
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756415
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444852
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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