A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012550



Internal ID19101767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1029678..1884167hg38UCSC Ensembl
Innerchr3:1071362..1925851hg19UCSC Ensembl
Innerchr3:1046362..1900851hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38854490
hg19854490
hg18854490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4618n100
Supporting Variantsnssv3590293
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)nsv1012550
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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