A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555835



Internal ID15996558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90218342..90336935hg38UCSC Ensembl
Innerchr11:89951510..90070103hg19UCSC Ensembl
Innerchr11:89591158..89709751hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38118594
hg19118594
hg18118594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2083n54
Supporting Variantsnssv780547
Samples
Known GenesCHORDC1, DISC1FP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555835
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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