A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3611330



Internal ID18909611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191156997..191277390hg38UCSC Ensembl
Innerchr3:190874786..190995179hg19UCSC Ensembl
Innerchr3:192357480..192477873hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38120394
hg19120394
hg18120394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012488
Supporting Variants
Samples
Known GenesOSTN, UTS2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3611330
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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