A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10476n54



Internal ID20143900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32004593..32029276hg38UCSC Ensembl
chr6:31972370..31997053hg19UCSC Ensembl
chr6:32080348..32105046hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3824684
hg1924684
hg1824699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602060, nsv602059, nsv602065, nsv602055, nsv602066, nsv602071, nsv602064, nsv602067
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)dgv10476n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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