A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv824582



Internal ID6137622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27694018..27702242hg19UCSC Ensembl
Innerchr8:27749937..27758161hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1429194
SamplesAK12
Known GenesPBK
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv824582
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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