A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933709



Internal ID21353778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101041048..101041048hg38UCSC Ensembl
chr11:100911779..100911779hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192311
SamplesHG002
Known GenesPGR
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933709
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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