A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046098



Internal ID18788629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:104336482..105132934hg38UCSC Ensembl
Innerchr11:104207210..105003661hg19UCSC Ensembl
Innerchr11:103712420..104508871hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38796453
hg19796452
hg18796452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517759
Samples
Known GenesCARD16, CARD17, CASP1, CASP12, CASP4, CASP5, LOC643733
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046098
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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