A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049881



Internal ID19139100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86174642..86187767hg38UCSC Ensembl
Innerchr11:85885684..85898809hg19UCSC Ensembl
Innerchr11:85563332..85576457hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3813126
hg1913126
hg1813126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1248n100
Supporting Variantsnssv3513447
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049881
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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