A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946303



Internal ID21366374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127071222..127071222hg38UCSC Ensembl
chr11:126941117..126941117hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191776
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946303
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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