A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361432



Internal ID22268811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122836537..122836537hg38UCSC Ensembl
chr11:122707245..122707245hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559215
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361432
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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