A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610868



Internal ID16051591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27884038..27924081hg38UCSC Ensembl
Innerchr8:27741555..27781598hg19UCSC Ensembl
Innerchr8:27797474..27837517hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3840044
hg1940044
hg1840044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109357
Samples
Known GenesMIR4287, SCARA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610868
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