A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004470



Internal ID19093688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:69547997..69679080hg38UCSC Ensembl
Innerchr3:69597148..69728231hg19UCSC Ensembl
Innerchr3:69679838..69810921hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38131084
hg19131084
hg18131084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594153
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)nsv1004470
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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