A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611957



Internal ID16399366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:113840898..113888338hg38UCSC Ensembl
Innerchr8:114853127..114900567hg19UCSC Ensembl
Innerchr8:114922303..114969743hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3847441
hg1947441
hg1847441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12274n54
Supporting Variantsnssv1119661, nssv1119662
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611957
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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