A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006724



Internal ID19095942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184474129..184555921hg38UCSC Ensembl
Innerchr3:184191917..184273709hg19UCSC Ensembl
Innerchr3:185674611..185756403hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3881793
hg1981793
hg1881793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5001n100
Supporting Variantsnssv3615005
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)nsv1006724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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