A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943110



Internal ID21363179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19618907..19618907hg38UCSC Ensembl
chr11:19640453..19640453hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190824
SamplesHG002
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943110
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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