A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615245



Internal ID16055968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114323095..114325155hg38UCSC Ensembl
Innerchr9:117085375..117087435hg19UCSC Ensembl
Innerchr9:116125196..116127256hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382061
hg192061
hg182061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12861n54
Supporting Variantsnssv1141272, nssv1141273, nssv1141274
Samples
Known GenesORM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615245
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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