A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936160



Internal ID21356230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45190788..45190788hg38UCSC Ensembl
chr19:45694046..45694046hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186534
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936160
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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