A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362152



Internal ID22116306
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224262
Supporting Variants
SamplesHG00512
Known GenesKIRREL3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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