A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610933



Internal ID16398342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:34792032..34852600hg38UCSC Ensembl
Innerchr8:34649550..34710118hg19UCSC Ensembl
Innerchr8:34769092..34829660hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3860569
hg1960569
hg1860569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12088n54
Supporting Variantsnssv1109990
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610933
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