A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614039



Internal ID16401448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29084710..29299062hg38UCSC Ensembl
Innerchr9:29084708..29299060hg19UCSC Ensembl
Innerchr9:29074708..29289060hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38214353
hg19214353
hg18214353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132294
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614039
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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