A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039617



Internal ID18782148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12273516..12324274hg38UCSC Ensembl
Innerchr11:12295063..12345821hg19UCSC Ensembl
Innerchr11:12251639..12302397hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3850759
hg1950759
hg1850759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508623
Samples
Known GenesMICALCL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039617
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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