A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006280



Internal ID19095498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176174406..176211916hg38UCSC Ensembl
Innerchr3:175892194..175929704hg19UCSC Ensembl
Innerchr3:177374888..177412398hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3837511
hg1937511
hg1837511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4991n100
Supporting Variantsnssv3614929
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)nsv1006280
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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