A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935200



Internal ID21355269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10798717..10798717hg38UCSC Ensembl
chr19:10909393..10909393hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186070
SamplesHG002
Known GenesDNM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935200
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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