A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949290



Internal ID21369360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77778115..77778115hg38UCSC Ensembl
chr11:77489161..77489161hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190938
SamplesHG002
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949290
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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