A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034412



Internal ID18776946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39104550..39273079hg38UCSC Ensembl
Innerchr9:39104547..39273076hg19UCSC Ensembl
Innerchr9:39094547..39263076hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38168530
hg19168530
hg18168530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7532n100
Supporting Variantsnssv3688944
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)nsv1034412
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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