A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042293



Internal ID18784824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112970023..112987859hg38UCSC Ensembl
Innerchr11:112840745..112858581hg19UCSC Ensembl
Innerchr11:112345955..112363791hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3817837
hg1917837
hg1817837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1279n100
Supporting Variantsnssv3506561
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)nsv1042293
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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