A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614735



Internal ID16055458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78030724..78032333hg38UCSC Ensembl
Innerchr9:80645640..80647249hg19UCSC Ensembl
Innerchr9:79835460..79837069hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381610
hg191610
hg181610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12772n54
Supporting Variantsnssv1137706
Samples
Known GenesGNAQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614735
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