A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038836



Internal ID19128055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106588947..106644047hg38UCSC Ensembl
Innerchr11:106459674..106514773hg19UCSC Ensembl
Innerchr11:105964884..106019983hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3855101
hg1955100
hg1855100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1272n100
Supporting Variantsnssv3710742
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)nsv1038836
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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