A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688909



Internal ID18640504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38989369..39273079hg38UCSC Ensembl
Innerchr9:38989366..39273076hg19UCSC Ensembl
Innerchr9:38979366..39263076hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38283711
hg19283711
hg18283711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035055
Supporting Variants
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)nssv3688909
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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