A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013396



Internal ID18755927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:944034..1373511hg38UCSC Ensembl
Innerchr3:985718..1415195hg19UCSC Ensembl
Innerchr3:960718..1390195hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38429478
hg19429478
hg18429478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4617n100
Supporting Variantsnssv3590291
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013396
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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