A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050802



Internal ID19140021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115392033..115458973hg38UCSC Ensembl
Innerchr11:115262751..115329692hg19UCSC Ensembl
Innerchr11:114767961..114834902hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3866941
hg1966942
hg1866942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517325
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)nsv1050802
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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