A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766442



Internal ID22100915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27489076..27489076hg38UCSC Ensembl
chr3:27530567..27530567hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381682
hg191682
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766442
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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