A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000284



Internal ID18742815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8780056..8811491hg38UCSC Ensembl
Innerchr3:8821742..8853177hg19UCSC Ensembl
Innerchr3:8796742..8828177hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3831436
hg1931436
hg1831436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4678n100
Supporting Variantsnssv3591859
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)nsv1000284
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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