A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033830



Internal ID19123051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143773621..143822893hg38UCSC Ensembl
Innerchr4:144694774..144744046hg19UCSC Ensembl
Innerchr4:144914224..144963496hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3849273
hg1949273
hg1849273
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5412n100
Supporting Variantsnssv3641201
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)nsv1033830
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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