A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14366334



Internal ID22273218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109661406..109661936hg38UCSC Ensembl
chr12:110099211..110099741hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557493
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14366334
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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