A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014364



Internal ID19103583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:72858423..72905870hg38UCSC Ensembl
Innerchr4:73724140..73771587hg19UCSC Ensembl
Innerchr4:73943004..73990451hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3847448
hg1947448
hg1847448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633818
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)nsv1014364
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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