A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10468n54



Internal ID22778363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31983430..32045574hg38UCSC Ensembl
chr6:31951207..32013351hg19UCSC Ensembl
chr6:32059186..32121329hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3862145
hg1962145
hg1862144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602027, nsv602026, nsv602033, nsv602011, nsv602043, nsv602044, nsv601997, nsv601981, nsv602014, nsv602040, nsv602032, nsv601996, nsv601998, nsv602037
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10468n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer