A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054408



Internal ID19143627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41872055..42025786hg38UCSC Ensembl
Innerchr11:41893605..42047336hg19UCSC Ensembl
Innerchr11:41850181..42003912hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38153732
hg19153732
hg18153732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522097
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)nsv1054408
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