A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038877



Internal ID18781408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:104166130..105422422hg38UCSC Ensembl
Innerchr11:104036858..105293149hg19UCSC Ensembl
Innerchr11:103542068..104798359hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381256293
hg191256292
hg181256292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507762, nssv3506920
Samples
Known GenesCARD16, CARD17, CARD18, 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)nsv1038877
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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