A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326493



Internal ID22131525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43175954..43185280hg38UCSC Ensembl
chr6:43143692..43153018hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg389327
hg199327
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3249149
Supporting Variants
SamplesHG00513
Known GenesCUL9, SRF
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326493
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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