A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928374



Internal ID21348443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43507400..43507400hg38UCSC Ensembl
chr19:44011552..44011552hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186180
SamplesHG002
Known GenesETHE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928374
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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