A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045851



Internal ID19135070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116606722..116636833hg38UCSC Ensembl
Innerchr11:116477439..116507550hg19UCSC Ensembl
Innerchr11:115982649..116012760hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3830112
hg1930112
hg1830112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517510
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)nsv1045851
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