A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445567



Internal ID22111745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79200138..79200138hg38UCSC Ensembl
chr13:79774273..79774273hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757935
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445567
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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