A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936460



Internal ID21356531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50811486..50811486hg38UCSC Ensembl
chr19:51314743..51314743hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186554
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936460
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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