A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018060



Internal ID18760593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39053783..39314111hg38UCSC Ensembl
Innerchr9:39053780..39314108hg19UCSC Ensembl
Innerchr9:39043780..39304108hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38260329
hg19260329
hg18260329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7530n100
Supporting Variantsnssv3688933
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018060
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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