A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041081



Internal ID18783612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:104927048..105041731hg38UCSC Ensembl
Innerchr11:104797775..104912458hg19UCSC Ensembl
Innerchr11:104302985..104417668hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38114684
hg19114684
hg18114684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710740
Samples
Known GenesCARD16, CASP1, CASP4, CASP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041081
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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