A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516564



Internal ID18468159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112966837..112987859hg38UCSC Ensembl
Innerchr11:112837559..112858581hg19UCSC Ensembl
Innerchr11:112342769..112363791hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3821023
hg1921023
hg1821023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054170
Supporting Variants
Samples
Known GenesNCAM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516564
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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