A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196269



Internal ID22346309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33085896..33087095hg38UCSC Ensembl
chr6:33053673..33054872hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327794, nssv14327790, nssv14327793, nssv14327791, nssv14327792, nssv14327795, nssv14327787, nssv14327788, nssv14327789
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesHLA-DPB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196269
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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