A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006379



Internal ID19095596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32461834..32546066hg38UCSC Ensembl
Innerchr4:32463456..32547688hg19UCSC Ensembl
Innerchr4:32107354..32191586hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3884233
hg1984233
hg1884233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620647
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)nsv1006379
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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