A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041778



Internal ID19130997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25877027..26076594hg38UCSC Ensembl
Innerchr11:25898574..26098141hg19UCSC Ensembl
Innerchr11:25855150..26054717hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38199568
hg19199568
hg18199568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513425
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)nsv1041778
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