A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506763



Internal ID18458358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115334028..115400481hg38UCSC Ensembl
Innerchr11:115204747..115271199hg19UCSC Ensembl
Innerchr11:114709957..114776409hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3866454
hg1966453
hg1866453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042473
Supporting Variants
Samples
Known GenesCADM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506763
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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