A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039134



Internal ID18781665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93056834..93486776hg38UCSC Ensembl
Innerchr11:92790000..93219942hg19UCSC Ensembl
Innerchr11:92429648..92859590hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38429943
hg19429943
hg18429943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507101
Samples
Known GenesCCDC67, SLC36A4, SMCO4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039134
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