A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928669



Internal ID21348739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126473080..126473080hg38UCSC Ensembl
chr11:126342975..126342975hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192834, nssv15192833
SamplesHG002
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928669
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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