A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614424



Internal ID16401833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67036224..67163322hg38UCSC Ensembl
Innerchr9:43659129..43790296hg19UCSC Ensembl
Innerchr9:43599125..43730292hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38127099
hg19131168
hg18131168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12716n54
Supporting Variantsnssv1134455, nssv1134451, nssv1134453, nssv1134450, nssv1134454, nssv1134452, nssv1134456
Samples
Known GenesCNTNAP3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614424
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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