A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610829



Internal ID16051552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25211884..25213015hg38UCSC Ensembl
Innerchr8:25069400..25070531hg19UCSC Ensembl
Innerchr8:25125317..25126448hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381132
hg191132
hg181132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107981
Samples
Known GenesDOCK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610829
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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