A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947920



Internal ID21367989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29696803..29696803hg38UCSC Ensembl
chr13:30270940..30270940hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193475
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947920
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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