A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613132



Internal ID16400541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2353522..2596783hg38UCSC Ensembl
Innerchr9:2353522..2596783hg19UCSC Ensembl
Innerchr9:2343522..2586783hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38243262
hg19243262
hg18243262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156436
Samples1780862125_A
Known GenesFLJ35024
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613132
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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