A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327792



Internal ID22234320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33085896..33087095hg38UCSC Ensembl
chr6:33053673..33054872hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196269
Supporting Variants
SamplesHG00733
Known GenesHLA-DPB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327792
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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