A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611487



Internal ID16398896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:70033364..70075574hg38UCSC Ensembl
Innerchr8:70945599..70987809hg19UCSC Ensembl
Innerchr8:71108153..71150363hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3842211
hg1942211
hg1842211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115776
Samples
Known GenesPRDM14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611487
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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