A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224262



Internal ID22367746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126921580..126921755hg38UCSC Ensembl
chr11:126791476..126791651hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1621n152
Supporting Variantsnssv14362152, nssv14362153
SamplesHG00512, HG00514
Known GenesKIRREL3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224262
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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