A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033695



Internal ID18776228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38996094..39273079hg38UCSC Ensembl
Innerchr9:38996091..39273076hg19UCSC Ensembl
Innerchr9:38986091..39263076hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38276986
hg19276986
hg18276986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7524n100
Supporting Variantsnssv3688927
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)nsv1033695
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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