A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440839



Internal ID22107017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36360274..36360274hg38UCSC Ensembl
chr13:36934411..36934411hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763644
Samples
Known GenesSPG20, SPG20OS
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440839
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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