A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949242



Internal ID21369313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69122018..69122018hg38UCSC Ensembl
chr6:69831910..69831910hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202808
SamplesHG002
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949242
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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