A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614056



Internal ID16401465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29150824..29496551hg38UCSC Ensembl
Innerchr9:29150822..29496549hg19UCSC Ensembl
Innerchr9:29140822..29486549hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38345728
hg19345728
hg18345728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132465
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer