A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5946n100



Internal ID22792033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32461817..32550980hg38UCSC Ensembl
chr6:32429594..32518757hg19UCSC Ensembl
chr6:32537572..32626735hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3889164
hg1989164
hg1889164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033457, nsv1023567, nsv1015397, nsv1022506
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5946n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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