A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048537



Internal ID18791068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8115806..8174656hg38UCSC Ensembl
Innerchr11:8137353..8196203hg19UCSC Ensembl
Innerchr11:8093929..8152779hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3858851
hg1958851
hg1858851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518215
Samples
Known GenesRIC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048537
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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