A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10625n54



Internal ID20144049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35496921..35497972hg38UCSC Ensembl
chr6:35464698..35465749hg19UCSC Ensembl
chr6:35572676..35573727hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381052
hg191052
hg181052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602918, nsv602920, nsv602917, nsv602919
Samples
Known GenesTEAD3, TULP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10625n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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