A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018148



Internal ID18760681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38796098..39089393hg38UCSC Ensembl
Innerchr9:38796095..39089390hg19UCSC Ensembl
Innerchr9:38786095..39079390hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38293296
hg19293296
hg18293296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688894
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)nsv1018148
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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