A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3740191



Internal ID19038472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65726020..65770325hg38UCSC Ensembl
Innerchr4:66591738..66636043hg19UCSC Ensembl
Innerchr4:66274333..66318638hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3844306
hg1944306
hg1844306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001623
Supporting Variants
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)nssv3740191
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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