A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040784



Internal ID18783315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:104893070..104985151hg38UCSC Ensembl
Innerchr11:104763797..104855878hg19UCSC Ensembl
Innerchr11:104269007..104361088hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3892082
hg1992082
hg1892082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506170
Samples
Known GenesCASP12, CASP4, LOC643733
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040784
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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