A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611848



Internal ID16399257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106834067..106881249hg38UCSC Ensembl
Innerchr8:107846295..107893477hg19UCSC Ensembl
Innerchr8:107915471..107962653hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3847183
hg1947183
hg1847183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118242
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611848
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