A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014304



Internal ID19103525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28142752..28154088hg38UCSC Ensembl
Innerchr3:28184243..28195579hg19UCSC Ensembl
Innerchr3:28159247..28170583hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3811337
hg1911337
hg1811337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589565
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)nsv1014304
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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