A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028147



Internal ID19117365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..59665hg38UCSC Ensembl
Innerchr5:15520..59780hg19UCSC Ensembl
Innerchr5:68520..112780hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3844146
hg1944261
hg1844261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5511n100
Supporting Variantsnssv3636499, nssv3636500
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)nsv1028147
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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