A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931847



Internal ID21351916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59645321..59645321hg38UCSC Ensembl
chr11:59412794..59412794hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190893
SamplesHG002
Known GenesPATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931847
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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