A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952743



Internal ID21372812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33218661..33218661hg38UCSC Ensembl
chr19:33709567..33709567hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186145
SamplesHG002
Known GenesSLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952743
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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