A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009196



Internal ID19098414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12375957..12673753hg38UCSC Ensembl
Innerchr4:12377581..12675377hg19UCSC Ensembl
Innerchr4:11986679..12284475hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38297797
hg19297797
hg18297797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5143n100
Supporting Variantsnssv3619833
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009196
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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