A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610666



Internal ID16398075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16604217..16655596hg38UCSC Ensembl
Innerchr8:16461726..16513105hg19UCSC Ensembl
Innerchr8:16506097..16557476hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3851380
hg1951380
hg1851380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12038n54
Supporting Variantsnssv1107302
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610666
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